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PQCM3815A2Home Blood Pressure Transmitter

Philips Medical Systems North America Co.
Home Blood Pressure Transmitter - FCC ID PQCM3815A2 - Philips Medical Systems North America Co.
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Application Details

Equipment Class
DXX - Part 15 Low Power Communication Device Transmitter
Date of Grant
Oct 16, 2001
Application Purpose
Original Equipment
Date of Application
Oct 16, 2001
Equipment Note
Home Blood Pressure Transmitter
Frequency Range
916.50000000 - 916.51000000
Company
Philips Medical Systems North America Co.
Country
United States

Documents & Files

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Users Manual

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Block Diagram

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Cover Letter(s)

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External Photos

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ID Label/Location Info

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Internal Photos

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Operational Description

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Test Report

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Test Setup Photos

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Document Text

Text extracted from the exhibit documents filed with the FCC. Open a document above to read the original.

Users Manual

Blood Pressure Unit User Guide M3815-90001-UG-Eng-revD.qxd 5/1/01 4:20 PM Page 1 Blood Pressure Unit Quick Start 2 Before You Start • Make sure you read and understand the Blood Pressure Unit User Guide. Taking Your Blood Pressure To begin, sit down, put on the blood pressure cuff, and press the START/STOPbutton. Your blood pressure (BP) is measured and displayed automatically. 1. Sit comfortably with your left forearm resting on a flat surface so that the center of your upper arm is at about the same height as your heart. 2. Loosen the blood pressure cuff so that you can slide the cuff over your arm. Place your hand into the cuff. 3. Slide the cuff up your forearm. 4. As you slide the cuff on, position the cuff so that the bottom of the cuff is on your upper arm and about one inch above the elbow crease; make sure that the air hose dangles on the inside of your arm. 5. Pull on the cuff end to tighten it. The cuff does not have to be pulled very tight. For comfort, you can leave room for one fin- ger to fit under the cuff. 6. Fold the cuff end back over the metal D-ring, and fasten the cuff end to the Velcro ® closure. 7. Press the START/STOPbutton. Sit still and do not move your arm during the measurement. If you want to stop the measure- ment at any time, press the START/STOP button. Wait 15 min- utes before taking your blood pressure again. M3815-90001-UG-Eng-revD.qxd 5/1/01 4:20 PM Page 2 3 BP User Guide 8. A series of numbers and symbols appear in the display window. The cuff inflates and may feel tight. A long beep signals the end of the BP measurement and the cuff deflates. The display window shows your final BP measurement and pulse rate. WARNING:As you watch the display, if you notice the pressure increase above 330 mmHg OR if the pressure decreases and remains at 15 mmHg for more than 3 minutes, press the START/STOPbut- ton to stop the measurement. The BP Unit is defective. Contact your Health Care Provider. 9. You can remove the cuff. The BP Unit has taken your blood pres- sure and pulse rate. The BP Unit turns off automatically. Note:Do not store the BP Unit with the air hose twisted or wrapped tightly around the display. M3815-90001-UG-Eng-revD.qxd 5/1/01 4:20 PM Page 3 Notice 4 The information contained in this document is subject to change without notice. Agilent Technologies makes no warranty of any kind with regard to this material, including, but not limited to, the implied warranties of mer- chantability and fitness for a particular purpose. Agilent Technologies shall not be liable for errors contained herein or for incidental or conse- quential damages in connection with the furnishing, performance, or use of this material. Agilent Technologies assumes no responsibility for the use or reliability of its software on equipment that is not furnished by Agilent Technologies. This document contains proprietary information that is protected by copyright. All rights are reserved. No part of this document may be photocopied, reproduced, or translated to another language without the prior written consent of Agilent Technologies. Copyright ©2001 Agilent Technologies, Inc. All rights reserved. Agilent Technologies, Inc. 3000 Minuteman Rd. Andover, MA 01810 USA Note: All Agilent devices must be initially installed by an Agilent installer or responsible party. The installation information provided in this guide is for reference only. M3815-90001-UG-Eng-revD.qxd 5/1/01 4:20 PM Page 4 Table of Contents 5 BP User Guide Blood Pressure Unit Quick Start ........................................2 Notice ....................................................................................4 Introduction ..........................................................................6 Precautions ............................................................................7 BP Unit Symbols ..................................................................9 BP Unit Components ..........................................................10 Installation ..........................................................................12 Installation Setup ..........................................................12 Inserting Four Type AA (1.5 Volt) Alkaline Batteries ........................................................................13 Performing a Radio Test................................................15 Preparing the Cuff Assembly ........................................17 How to Take Your Blood Pressure ....................................18 Taking Your Blood Pressure..........................................19 What Display Symbols Mean ............................................26 Maintenance ........................................................................27 Troubleshooting ..................................................................28 Specifications ......................................................................30 Electromagnetic Compatibility ........................................32 Electromagnetic Compatibility Testing ....................32 Avoiding Electromagnetic Interference Problems ..33 FCC Regulations ................................................................34 Conclusion ..........................................................................35 M3815-90001-UG-Eng-revD.qxd 5/1/01 4:20 PM Page 5 6 Welcome to Agilent Technologies’ Interactive Healthcare Services. Your Health Care Provider has enrolled you in a progressive program to mea- sure, transmit, and review your vital signs on a daily basis. This pro- gram’s approach will help you and your provider make better informed decisions about your care. Your patient measurement set—which may include a Scale, Blood Pressure Unit, Rhythm Strip Recorder, and Home Hub—is designed to let you quickly and easily take your vital signs. The data you collect in a few minutes each day are automatically transferred via the Agilent Home Hub, using your existing phone line, to your Health Care Provider’s computer system. The H…

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Block Diagram

A A B B C C D D E E 44 33 22 11 Antenna in PCB etch RFM TR1000 Transmitter enable/sleep Transmit serial stream Matching network Transmit level-set components Transmit level select (Normal/Reduced) RF block diagram A2 AND BP Interface: M3815-20300 A 11Thursday, September 06, 2001 eCare Services 3500 Deer Creek Rd., Palo Alto, CA 94304 Philips CONFIDENTIAL Title SizeDocument NumberRev Date:Sheet of

Cover Letter(s)

Federal Communications Commission 7435 Oakland Mills Road Columbia, MD 21046 Gentlemen: This letter is to comply with 47 CFR 0.457(d)(2)(I) pertaining to confidential material. Philips Medical Systems requests that the following documents regarding this submission for FCC ID PQCM3815A2 be kept confidential: 1. Schematic 2. Bill of Materials The material above contains technical data, which would customarily be guarded from competitors. We at Curtis-Straus LLC are acting as an Agent on behalf of Philips Medical Systems in requesting confidentiality with regards to the preceding documents. Sincerely, Michael Buchholz Senior EMC Manager Curtis-Straus LLC 527 Great Road Littleton, MA 01460

External Photos

External Photos Philips Medical Systems M3815A FCC ID: PQCM3815A2 Note: These pictures were taken before the official name change from Agilent to Philips. The label has since been changed to reflect the current company name. Philips Medical Systems M3815A FCC ID: PQCM3815A2

Internal Photos

Internal Photos Philips Medical Systems M3815A FCC ID: PQCM3815A2 Philips Medical Systems M3815A FCC ID: PQCM3815A2 Philips Medical Systems M3815A FCC ID: PQCM3815A2

Operational Description

Description of the Philips Home Blood Pressure Transmitter circuit Robert C. Leichner 6 September 2001 The M3815 Blood Pressure transmitter circuit is based on R. F. Monolithics (RFM) TR1000 hybrid transceiver module. Printed circuit board load options have been selected to constrain the transceiver to three operating modes. The operating mode in effect at any given time is selected by the device microprocessor. The available modes are Standby, Transmit, and Test. • Standby mode is a very low power consumption state in which the transceiver consumes absolute minimum power, and emits no RF energy. • Transmit mode is constrained, again by load options, to ON-OFF keying. Transmit mode is the normal mode for transfer of measurement and status messages. Transmit mode is used during FCC part 15 testing. • Test mode is identical to Transmit mode except that RF output is reduced by approximately 3 dB. Test mode – rarely used - is used during device installation, and to verify RF link operation. Characteristics of the 19.6kilobit serial data stream that modulates the TR1000 output in Transmit and Test modes are presented elsewhere in the FCC 15.249 submission. Quoting from the RFM TR1000 data sheet: TR1000 916.50 MHz Hybrid Transceiver The TR1000 hybrid transceiver is ideal for short-range wireless data applications where robust operation, small size, low power consumption and low cost are required. The TR1000 employs RFM’s amplifier-sequenced hybrid (ASH) architecture to achieve this unique blend of character-istics. All critical RF functions are contained in the hybrid, simplifying and speeding design-in. The receiver section of the TR1000 is sensitive and stable. A wide dynamic range log detector, in combination with digital AGC and a compound data slicer, provide robust performance in the presence of on-channel interference or noise. Two stages of SAW filtering provide excellent receiver out-of-band rejection. The transmitter includes provisions for both on-off keyed (OOK) and amplitude-shift keyed (ASK) modulation. The transmitter employs SAW filtering to suppress output harmonics, facilitating compliance with FCC 15.249 and similar regulations. The TR1000 transmitter output power is determined by current flowing into TXMOD (pin 8 of the TR1000). The transmitter design supports both Transmit mode used to transfer Blood Pressure measurement results and status messages, as well as a reduced power test mode. R74 and R75 control the current into TR1000 pin 8 in the higher power normal mode. The two resistors are used in series to allow the combined resistance, and the resulting power level, to be set with greater precision than possible using a single standard resistor value. The data signal driving the resistors and the TR1000 TXMOD input is the output of a 74HC00 quad NAND gate. The 74HC00 output is lightly loaded by the transmitter, and when driven, will be stable and close to the power supply voltage. The power supply voltage is controlled by a linear regulator (Micrel MIC5219-3.0BM5) with better than 1% output load regulation and worst case accuracy of 2%. In combination, these factors result in a well-controlled drive signal to the RFM TR1000. R76 modifies the drive to the TXMOD pin by diverting a portion of the available drive current when RFattenuate- is asserted (LOW). Current into TXMOD, and the resulting TR1000 output level, are reduced when Rfattenuate- is asserted. R76 was selected to produce a 3dB drop in RF output level. D4 is reverse biased during Transmit mode assuring that R76 is isolated from the transmitter during non-test operation.

Test Report

MEASUREMENT/TECHNICAL REPORT Company: Philips Medical Systems Model: M3815A FCC ID: PQCM3815A2 October 9, 2001 Description: This is a report to support a request for an original grant of equipment authorization. Equipment Type: Low Power Communications Device Transmitter (DXX) Report prepared for: Philips Medical Systems 3500 Deer Creek Road Palo Alto, CA 94304 Phone: (650) 857-8720 Fax: (650) 236-9981 Report prepared by: Evan D. Gould Curtis-Straus LLC 527 Great Road Littleton, MA 01460 USA Phone: 978-486-8880 FAX: 978-486-8828 FCC Application for Philips Medical Systems••FCC ID: PQCM3815A2 •• Report No. EB0911-1 10-Oct-01 ______________________________________________________________________ _____________________________ ________________________________ Curtis-Straus LLC •• 527 Great Road •• Littleton, MA •• TEL (978) 486-8880 •• FAX (978) 486-8828 page 2 of 9 Introduction This report is an application for Certification of a Transmitter operating pursuant to Part 15.249 of the FCC Rules, Code of Federal Regulations 47. The model number covered by this report is M3815A. This report is designed to demonstrate the compliance of this device with the requirements outlined in Part 15 of CFR 47 using the methods outlined in Part 2 of CFR 47. The confidential information and descriptions included in this application are detailed descriptions of the products, block diagrams, component specifications, and schematic diagrams. We hereby respectfully request under the provision of section 0.457d of the code that the documents listed below be held confidential. Schematics Bill of Materials FCC Application for Philips Medical Systems••FCC ID: PQCM3815A2 •• Report No. EB0911-1 10-Oct-01 ______________________________________________________________________ _____________________________ ________________________________ Curtis-Straus LLC •• 527 Great Road •• Littleton, MA •• TEL (978) 486-8880 •• FAX (978) 486-8828 page 3 of 9 Statement of Conformity The Philips Medical Systems M3815A has been found to conform with the following parts of the 47 CFR as detailed below: Part 2 Part 15 Comments 15.15(b) The product contains no user accessible controls that increase transmission power above allowable levels. 2.925 15.19 The label is shown in the label exhibit. 15.21 Information to the user is shown in the instruction manual exhibit. 15.27 No special accessories are required for compliance. 15.203 The antenna is built into the board and there is no external antenna connection. 15.205 15.209 The fundamental is not in a Restricted band and the spurious and harmonic emissions in the Restricted bands comply with the general emission limits of 15.209. 15.207 The unit is battery powered without the capability of being recharged or operated from the AC mains. 15.249(a) The unit complies with the field strength limits of the 15.249(a) table including the 20dB peak restriction of 15.35(b) and 15.249(d). 15.249(c) The unit complies with the field strength limits of the 15.209(a) table. FCC Application for Philips Medical Systems••FCC ID: PQCM3815A2 •• Report No. EB0911-1 10-Oct-01 ______________________________________________________________________ _____________________________ ________________________________ Curtis-Straus LLC •• 527 Great Road •• Littleton, MA •• TEL (978) 486-8880 •• FAX (978) 486-8828 page 4 of 9 Test Methodology Radiated emission testing was performed according to the procedures in ANSI C63.4 (1992). The testing was performed at an antenna to EUT distance of 3 or 10 meters below 1 GHz, and at a distance of 3 or 1 meter(s) above 1 GHz. The actual test distance used is noted in the test data sheets. The device’s performance was investigated to 10GHz. The EUT was powered by four Duracell PC1500 PROCELL 1.5Volt AA batteries. Fresh batteries were used for all testing. The circuit board was hardwired so as to produce a continuous transmission signal as opposed to the momentary transmission that occurs during regular operation. Since the device is a table- top unit, the emissions were maximized around the vertical axis and the maximum reading was recorded. The integrated antenna cannot be maximized separately. All other performance tests were made in accordance with the procedures outlined in Part 15 of CFR 47. The applicable sections provided under Part 15 are provided in the measurement section of this report. FCC Application for Philips Medical Systems••FCC ID: PQCM3815A2 •• Report No. EB0911-1 10-Oct-01 ______________________________________________________________________ _____________________________ ________________________________ Curtis-Straus LLC •• 527 Great Road •• Littleton, MA •• TEL (978) 486-8880 •• FAX (978) 486-8828 page 5 of 9 Test Facility Curtis-Straus LLC All testing for the range 30–10,000MHz was performed at Curtis-Straus (A2LA Certificate Number 1627-01). The open area test site used to collect the radiated data is located at 527 Great Road, Littleton, MA 01460. Site “T” and “F” were used. FCC Application for Philips Medical Systems••FCC ID: PQCM3815A2 •• Report No. EB0911-1 10-Oct-01 ______________________________________________________________________ _____________________________ ________________________________ Curtis-Straus LLC •• 527 Great Road •• Littleton, MA •• TEL (978) 486-8880 •• FAX (978) 486-8828 page 6 of 9 Test Equipment Used SPECTRUM ANALYZERS x Analyzer Model No. Company Serial No. Calibration Due X YELLOW 9kHz-2.9GHz 8594E HP 3523A01958 27-JUL-2002 X GREEN 9kHz-26.5GHz 8593E HP 3829A03618 05-OCT-2001 X ORANGE 9kHz-26.5GHz E4407B HP US39440975 18-MAY-2002 OPEN AREA TEST SITES (OATS) x Site FCC Code IC Code VCCI Code Calibration Due X “F” Florida 93448 IC 2762-F R-468/ C-480 23-JUN-2002 X “T” Texas 93448 IC 2762-T R-905/ C-480 09-SEP-2002 ANTENNAS x Antenna Model No. Company Serial No. Calibration Due X GREEN-BLACK Bilog: 30MHz-2GHz CBL6112B Chase 2412 28-JUN-2002 X RED Bilog: 30MHz-1GHz 3143 EMCO 1270 28-JUN-2002 X BLACK Horn: 1-18GHz 3115 EMCO 9703-5148 12-J…

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Contact Information

Applicant

Delroy Smith(Principal Architect)
[email protected]1-617-798-0865Fax: 1-617-798-0865

Test Firm

Curtis-Straus LLCJonathan Stewart
[email protected]978-486-8880Fax: 978-486-8828

Technical Specifications

#Rule PartsFrequency RangePower Output
115C916.5 MHz - 916.51 MHz-
Confidentiality
Long Term
Grant Notes
Certified under Part 15.249

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