MICROLIFE DIGITAL INFRARED EAR THERMOMETER, MODEL IR1DE1

K020725 · Microlife Corp. · FLL · Mar 12, 2002 · General Hospital

Device Facts

• Record ID: K020725
• Device Name: MICROLIFE DIGITAL INFRARED EAR THERMOMETER, MODEL IR1DE1
• Applicant: Microlife Corp.
• Product Code: FLL · General Hospital
• Decision Date: Mar 12, 2002
• Decision: SESE
• Submission Type: Special
• Regulation: 21 CFR 880.2910
• Device Class: Class 2
• Attributes: Pediatric

Intended Use

The device is an electronic clinical thermometer using an infrared sensor to detect body temperature from the auditory canal in the neonatal, pediatric and adult population used in the home setting.

Device Story

Electronic infrared ear thermometer; uses thermopile sensor to detect natural thermal radiation from tympanic membrane and adjacent surfaces. Device components include IR thermopile sensor, ASIC, E2 PROM IC, LCD with backlight, and buzzer. Operated by user in home setting; provides temperature measurement via 1-second 'normal' mode. Output displayed on LCD; assists users in monitoring body temperature. Modifications from predicate include external ergonomics, dimensional specifications, and PCB layout; temperature measurement algorithm and software remain unchanged.

Clinical Evidence

No clinical studies were conducted for the modified device. Substantial equivalence is supported by bench testing, including compliance with ASTM E1112, ASTM E1104, ASTM E-1965-98, IEC 60601-1, and IEC 60601-1-2. Accuracy, reliability, and EMC testing were performed.

Technological Characteristics

Infrared thermopile sensor; ASIC and E2 PROM IC components. Standards: ASTM E1112, ASTM E1104, ASTM E-1965-98, IEC 60601-1, IEC 60601-1-2. 1-second measurement mode. Standalone device.

Indications for Use

Indicated for neonatal, pediatric, and adult populations for the measurement of body temperature via the auditory canal in a home setting.

Regulatory Classification

Identification

A clinical electronic thermometer is a device used to measure the body temperature of a patient by means of a transducer coupled with an electronic signal amplification, conditioning, and display unit. The transducer may be in a detachable probe with or without a disposable cover.

Special Controls

(1) Device is not a clinical thermometer with telethermographic functions; (2) Device is not a clinical thermometer with continuous temperature measurement functions; and (3) Appropriate analysis and testing (such as that outlined in the currently FDA-recognized editions, as appropriate, of ISO 80601-2-56, “Medical electrical equipment—Part 2-56: Particular requirements for basic safety and essential performance of clinical thermometers for body temperature measurement,” or ASTM E1965, “Standard Specification for Infrared Thermometers for Intermittent Determination of Patient Temperature,” or ASTM E1112, “Standard Specification for Electronic Thermometer for Intermittent Determination of Patient Temperature,” or ASTM E1104, “Standard Specification for Clinical Thermometer Probe Covers and Sheaths”) must validate specifications and performance of the device.

Predicate Devices

• Microlife Digital Infrared Ear Thermometer, Model IR1DA1 (K000969, K003308)

Submission Summary (Full Text)

{0}------------------------------------------------

# EXHIBIT #1

K020725

# 510(K) SUMMARY

This summary of 5l0(k) safety and effectiveness information is being submitted in accordance with the requirements of SMDA 1990 and 21 CFR §807.92.

The assigned 5l0(k) number is: _______________________________________________________________________________________________________________________________________________

## 1. Submitter's Identification:

Microlife Corporation 9F, 431 Rui Guang Road Nei Hu. Taipei 114 Taiwan, Republic of China

Date Summary Prepared:

March 4, 2002

## 2. Name of the Device:

Microlife Digital Infrared Ear Thermometer, Model IR1DE1.

## Information for the 510(k) Cleared Device (Predicate Device): 3.

Microlife Digital Infrared Ear Thermometer, Model IR1DA1, K#000969, K#003308.

## 4. Device Description:

The Microlife Digital Infrared Ear Thermometer, Model IR1DE1 is an electronic thermometer using an infrared sensor (thermopile) to detect body temperature from the auditory canal. Their operation is based on measuring the natural thermal radiation emanating from the tympanic membrane and the adjacent surfaces.

The Microlife Digital Infrared Ear Thermometer, consists mainly of the five parts:

- IR Thermopile Sensor a)
- ASIC b)
- E2 PROM IC C)

{1}------------------------------------------------

- LCD and Blacklight d)
- Kev "2. Buzzer" 1 e)

## 5. · Intended Use:

The device is an electronic clinical thermometer using an infrared sensor to detect body temperature from the auditory canal in the neonatal, pediatric and adult population used in the home setting.

## 6. Comparison to the 510(k) Cleared Device (Predicate Device):

The Microlife Digital Infrared Ear Thermometer, Model IR1DE1 is substantially equivalent to the original Microlife Digital Ear Thermometer, Model IR1DA1.

The new model IR1DE1 has the same intended use and is similar in design to the 510(k) cleared device.

The IR1DE1 and the IR1DA1 are identical in functionality and performance with the only difference being the external shape of the devices, and PCB layout of the devices. The modifications to our original 510(k) cleared device, model IR1DA1, include ergonomics of the user interface, dimensional specifications and environmental specifications. The temperature measurements algorithm and its software codes of the modified devices remains unchanged. The fundamental scientific technology of the modified device remains the same as that of the 510(k) cleared device. The Microlife device (IR1DE1) works with only a 1second called a "normal" mode.

## 7. Discussion of Non-Clinical Tests Performed for Determination of Substantial Equivalence are as follows:

Compliance to applicable voluntary standards includes ASTM E1112, ASTM E1104 and ASTM E-1965-98, as well as IEC 60601-1 and IEC 60601-1-2 requirements.

Guidance documents included the "FDA Guidance On The Content of Premarket Notification (510(k)) Submissions for Clinical Electronic Thermometers", "Deciding When to Submit a 510(k) for a Change to An Existing Devices", and, "The New 510(k) Paradigm: Alternate Approaches to Demonstrating Substantial Equivalence in Premarket Notifications".

{2}------------------------------------------------

## 8. Discussion of Clinical Tests Performed:

Controlled human clinical studies were not conducted for the Microlife Digital Infrared Ear Thermometer modified devices, as well as no low power test as clinical studies/low power testing were conducted for the original unmodified device and remain unchanged. Accuracy performance, reliability and EMC testing is only applicable.

## 9. Conclusions:

The Microlife Digital Infrared Ear Thermometer, Model IR1DE1 has the same intended use and technological characteristics as the unmodified model IR1DA1. Moreover, verification and validation tests contained in this submission demonstrate that the modified portions maintained its original safety and effectiveness. These engineering changes do not: (1) affect the intended use or (2) alter the fundamental scientific technology of the device.

{3}------------------------------------------------

Image /page/3/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a circular seal with the words "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA" arranged around the perimeter. Inside the circle is an abstract symbol resembling an eagle or bird in flight, composed of three stylized, curved lines.

Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

# MAR 1 2 2002

MicroLife Corporation C/O Ms. Susan D. Goldstein-Falk MDI Consultants, Incorporated 55 Northern Boulevard, Suite 200 Great Neck, New York 11021

Re: K020725

Trade/Device Name: Microlife Digital Infrared Ear Thermometer, Model IR1DE1 Regulation Number: 880.2910 Regulation Name: Clinical Electronic Thermometer Regulatory Class: II Product Code: FLL Dated: March 4, 2002 Received: March 6, 2002

Dear Ms. 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.

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.

{4}------------------------------------------------

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 and additionally 21 CFR Part 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at [phone]. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at [phone]. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number [phone] or [phone] or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html

Sincerely yours,

Timothy A. Ulatowski Director Division of Dental, Infection Control and General Hospital Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

{5}------------------------------------------------

Exhibit B

#### Page of 1 r

510(k) Number (if known): K020725

Device Name: Microlife Digital Infrared Ear Thermometer, Model IR1DE1

## Indications For Use:

The device is an electronic clinical thermometer using an infrared sensor to detect body temperature from the auditory canal in the neonatal, pediatric and adult population used in the home setting.

# (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)

# Concurrence of CDRH, Office of Device Evaluation (ODE)

Prescription Use (Per 21 CFR 801.109)

OR

**Over-The-Counter Use**
(Optional Format 1-2-96)

Patricio Cussenite

(Division Sign-Off) Division of Dental, Infection Control, and General Hospital Devices F10(k) Number _ K- 020225