PM-50 PULSE OXIMETER AND VS-800 VITAL SIGNS MONITOR
Device Facts
| Record ID | K072235 |
|---|---|
| Device Name | PM-50 PULSE OXIMETER AND VS-800 VITAL SIGNS MONITOR |
| Applicant | Shenzhen Mindray Bio-Medical Electronics Co., Ltd. |
| Product Code | DQA · Cardiovascular |
| Decision Date | Oct 19, 2007 |
| Decision | SESE |
| Submission Type | Special |
| Regulation | 21 CFR 870.2700 |
| Device Class | Class 2 |
| Attributes | Pediatric |
Indications for Use
The PM-50 Pulse Oximeter is a non-invasive, spot-check, oxygen saturation and pulse rate monitor. It operates only on battery power using existing PM-50 disposable and reusable sensors labeled for patients ranging from neonates to adults. The VS-800 Vital Signs Monitor is used to monitor physiologic parameters including SpO2, PR and NIBP, and to measure Temperature parameter on adult, pediatric, and neonatal patients in healthcare facilities by clinical physicians or appropriate medical staff under the direction of physicians. It is not intended for transport or home use.
Device Story
PM-50: Portable, battery-powered pulse oximeter; uses two-wavelength (red/infrared) pulsatile system to measure SpO2 and pulse rate via finger sensor; displays values on LCD. VS-800: Configurable vital signs monitor; measures SpO2, PR, NIBP, and temperature; powered by AC mains or internal battery (lead-acid/lithium); features LCD/LED display, menu-driven interface, and optional thermal recorder. Used in healthcare facilities by clinicians; provides audible/visual alarms for parameter violations. Both devices utilize existing sensor technology to provide real-time physiological data for clinical decision-making.
Clinical Evidence
Clinical study conducted according to ISO9919 to validate SpO2 performance following probe modification. Bench testing included design change analysis, biocompatibility, performance, and safety/EMC testing. Results demonstrated devices meet design specifications and perform equivalently to predicates.
Technological Characteristics
PM-50: Portable, battery-powered. VS-800: AC/battery-powered (lead-acid/lithium). Both use two-wavelength (red/infrared) optical sensing for SpO2. VS-800 includes NIBP and temperature modules. Connectivity via patient cables; optional thermal recorder. Software-based parameter processing and alarm management.
Indications for Use
Indicated for monitoring SpO2, pulse rate, NIBP, and temperature in adult, pediatric, and neonatal patients in healthcare facilities. Not for transport or home use.
Regulatory Classification
Identification
An oximeter is a device used to transmit radiation at a known wavelength(s) through blood and to measure the blood oxygen saturation based on the amount of reflected or scattered radiation. It may be used alone or in conjunction with a fiberoptic oximeter catheter.
Predicate Devices
Submission Summary (Full Text)
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OCT 1 9 2007
# 510(K) SUMMARY
This summary of 510(k) safety and effectiveness information is being submitted in accordance with the requirements of SMDA 1990 and 21 CFR §807.92.
The assigned 510(k) number is:
## Submitter:
Shenzhen Mindray Bio-medical Electronics Co., LTD Mindray Building, Keji 12th Road South, Hi-tech Industrial Park, Nanshan, Shenzhen, 518057, P. R. China
Tel: +86 755 2658 2888 Fax: +86 755 2658 2680
- Contact Person: .
Li Dongling Shenzhen Mindray Bio-medical Electronics Co., LTD Mindray Building, Keji 12th Road South, Hi-tech Industrial Park, Nanshan, Shenzhen, 518057, P. R. China
- Date Prepared: .
July 31, 2007
## Name of the device:
| Trade/Proprietary Name | PM-50 Pulse Oximeter | VS-800 Vital Signs Monitor |
|------------------------|------------------------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Common Name | Pulse Oximeter | Vital Signs Monitor |
| Classification | 21 CFR 870.2700, Oximeter, Pulse, 74 DQA<br>21 CFR 870.2710, Ear Oximeter, Pulse, 74 DQA | 21 CFR 870.2700, Oximeter, Pulse, 74 DQA<br>21 CFR 870.2710, Ear Oximeter, Pulse, 74 DQA<br>21 CFR 870.2300, Cardiac monitor (including cardiotachometer and rate alarm), 74 MWI<br>21 CFR 870.1130, Non-Invasive blood pressure measurement System ,74 DXN<br>21 CFR 880.2910, Clinical Electronic Thermometer, 80 FLL |
| Predicate Device | K061442, PM-50 Pulse Oximeter, cleared on Sep 5, 2006 | K063055, VS-800 Vital Signs Monitor, cleared on Dec 21, 2006 |
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#### Device Description:
PM-50 Pulse Oximeter:
The PM-50 is a flexible, portable, battery powered Pulse Oximeter. The PM-50 Pulse Oximeter acquires the physiological signals - oxygen saturation (SpO2) and pulse rate (PR). The signals are converted into digital data and processed, and the SpO2 and pulse rate values are calculated and displayed on LCD screen.
PM-50 uses a two-wavelength pulsatile system - red and infrared light - to obtain SpO2 based on the different light absorption of oxygenated and reduced hemoglobin. The light source in the finger sensor emits red and infrared light, which are partially absorbed and modulated by the arterial blood pulsation at the sensor site. The photodetector in finger sensor collects and converts the light into electronic signal which is proportional to the light intensity. The electronic signals are sent to the oximeter and processed by the oximeter's circuitry. Thereafter, the SpO2 and pulse rate are obtained and indicated on the LCD screen.
VS-800 Vital Signs Monitor:
The VS-800 Vital Signs Monitor is a prescription device intended for use by health care professionals. And the device is capable of operation from an external AC mains powers source or an internal battery including rechargeable lead-acid battery and lithium battery. The device uses the same or similar technology and materials as the predicate devices, see Legally Marketed Predicate Devices listed above.
The VS-800 Vital Signs Monitor is a configurable monitor with options selected by customer preference. Device's options including module configuration and language setting are configured at the time the monitor is manufactured. Options may be upgrade via upgrade port by the manufacturer. The monitor also provides customer with the convenient operating control and human-machine interface (HMI). All of the patient cable connections are located on the monitor. The LCD and LED display patient information and the menu provides single control operations of all main functions. Operator can adjust parameter alarm settings that give audible and visual indication when a violation occurs. The VS-800 provides option for printing information by a thermal recorder.
This monitor has the following parameters measurement functions:
- V SpO2 measurement: pulse oxygen saturation (SpO2), pulse rate (PR), and SpO2 plethysmogram.
- イ NIBP measurement: systolic pressure (S), diastolic pressure (D), mean pressure (M), and pulse rate (PR).
- V Rectal / oral / axillary TEMP measurement: temperature (TEMP).
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## Intended Use:
The PM-50 Pulse Oximeter is a non-invasive, spot-check, oxygen saturation and pulse rate monitor. It operates only on battery power using existing PM-50 disposable and reusable sensors labeled for patients ranging from neonates to adults.
The VS-800 Vital Signs Monitor is used to monitor physiologic parameters including SpO2, PR and NIBP, and to measure Temperature parameter on adult, pediatric, and neonatal patients in healthcare facilities by clinical physicians or appropriate medical staff under the direction of physicians. It is not intended for transport or home use.
# Comparison of Technological Characteristics:
The PM-50 Pulse Oximeter and VS-800 Vital Signs Monitor employ the same functional technology as the predicate devices.
### Testing:
The device modification only involved the addition of SpO2 probes to PM-50 Pulse Oximeter and VS-800 Vital Signs Monitor. Bench testing and clinical study was conducted based on the modification to verify and validate that the PM-50 Pulse Oximeter and VS-800 Vital Signs Monitor met all design specifications and were substantially equivalent to predicate devices.
The following quality assurance measures were applied to the devices:
- Design Change and Modification Influence Analysis
- Biocompatibility Testing
- Performance Testing
- Safety & Environmental &EMC Testing
- Clinical Study according to ISO9919
### Conclusion:
The conclusions drawn from clinical and bench testing of the PM-50 Pulse Oximeter and VS-800 Vital Signs Monitor demonstrate that the devices is as safe, as effective, and performs as well as the predicate devices.
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Image /page/3/Picture/1 description: The image shows the logo for the U.S. Department of Health and Human Services. The logo consists of a stylized caduceus symbol, which is a staff with two snakes coiled around it, and the words "DEPARTMENT OF HEALTH AND HUMAN SERVICES. USA" arranged in a circle around the symbol. The caduceus symbol is composed of four abstract human figures, each with their head bowed. The logo is black and white.
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
OCT 1 9 2007
Shenzhen Mindray Bio-Medical Electronics Company, Limited C/O Ms. Susan D. Goldstein-Falk Official Correspondent MDI Consultants, Incorporated 55 Northern Boulevard, Suite 200 Great Neck, New York 11021
Re: K072235
Trade/Device Name: PM-50 Pulse Oximeter and VS-800 Vital Signs Monitor Regulation Number: 870.2700 Regulation Name: Oximeter Regulatory Class: II Product Code: DQA Dated: September 13, 2007 Received: September 19, 2007
Dear Ms. Goldstein-Falk:
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
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Page 2 - Ms. Goldstein-Falk
Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
This letter will allow you to begin marketing your device as described in your Section 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Office of Compliance at (240) 276-0120. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html.
Sincerely vours.
Chiu Lin, Ph.D.
Chiu Lin, Ph.D Director
Division of Anesthesiology, General Hospital, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
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# Indications for Use
510(k) Number (if known):
Device Name: PM-50 Pulse Oximeter and VS-800 Vital Signs Monitor Indications For Use:
The PM-50 Pulse Oximeter is a non-invasive, spot-check, oxygen saturation and pulse rate monitor. It operates only on battery power using existing PM-50 disposable and reusable sensors labeled for patients ranging from neonates to adults.
The VS-800 Vital Signs Monitor is used to monitor physiologic parameters including SpO2, PR and NIBP, and to measure Temperature parameter on adult, pediatric, and neonatal patients in healthcare facilities by clinical physicians or appropriate medical staff under the direction of physicians. It is not intended for transport or home use.
Prescription Use X (Part 21 CFR 801 Subpart D)
AND/OR
Over-The-Counter Use (21 CFR 801 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
Mull Whil
Control, Dental Devices
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Number: K072235
nesthesiology, General Hospital.
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