TEMPTOUCH DERMAL THERMOMETER

K081162 · Diabetica Solutions, Inc. · FLL · May 8, 2008 · General Hospital

Device Facts

Record IDK081162
Device NameTEMPTOUCH DERMAL THERMOMETER
ApplicantDiabetica Solutions, Inc.
Product CodeFLL · General Hospital
Decision DateMay 8, 2008
DecisionSESE
Submission TypeTraditional
Regulation21 CFR 880.2910
Device ClassClass 2
AttributesPediatric, 3rd-Party Reviewed

Indications for Use

The TempTouch® is an infrared thermometer intended for the intermittent measurement and monitoring of human skin surface temperature in the home or clinic for use with people of all ages.

Device Story

Handheld, 9V battery-operated infrared thermometer; measures natural thermal infrared radiation emitted from skin surface. Uses thermopile infrared sensor transducer; electronic signal amplification and conditioning; LCD display. Operated by clinicians or patients in home/clinic. Provides skin surface temperature readings to assist in monitoring. Non-invasive measurement.

Clinical Evidence

Bench testing only. Performance tests included accuracy, repeatability, °F vs. °C conversion, variable voltage, and error message functionality. All tests passed.

Technological Characteristics

Thermopile infrared sensor transducer; electronic signal amplification and conditioning; LCD display; 9V battery-powered; handheld form factor.

Indications for Use

Indicated for intermittent measurement of skin surface temperature in patients of all ages in home or clinical settings.

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

Submission Summary (Full Text)

{0}------------------------------------------------ 510(k) Summary | Submitter: | Diabetica Solutions Inc.<br>12665 Silicon Drive<br>San Antonio, TX 78249<br>(210) 692-1114 Telephone<br>(210) 692-1144 Fax | K081162 (P.1 of 2)<br><br>MAY - 8 2008 | |----------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|----------------------------------------| | Contact Person: | J. B. Allinson Jr. | | | Date of Summary: | February 28, 2008 | | | Trade Name: | TempTouch® Dermal Thermometer | | | Common Name: | Skin Surface Thermometer | | | Device Description: | The TempTouch® is a handheld, 9V battery-operated device<br>that measures the surface temperature of the skin. Operation<br>is based on measuring the natural thermal infrared radiation<br>emitted from the surface of the skin. | | | Intended Use: | The TempTouch® is an infrared thermometer intended for<br>the intermittent measurement and monitoring of human<br>skin surface temperature in the home or clinic for use with<br>people of all ages. | | | Classification: | Clinical Electronic Thermometer<br>Product Code: FLL<br>Regulation No. 880.2910<br>Class: II<br>Panel: 80 (General Hospital) | | | Predicate Device(s): | Omega Surface Temperature Scanner<br>(K873010)<br>Temp Touch Dermal Thermometer<br>(K050137) | | | Technical Characteristics: | The TempTouch® Thermometer and the predicate devices<br>are used to measure the temperature of a human by means<br>of a thermopile infrared sensor transducer coupled with<br>electronic signal amplification, conditioning, and a display<br>unit | | · {1}------------------------------------------------ ## KABI162 (0,2002) The Omega predicate employs solid- state electronic signal amplification, which is technology similar to the electronic surface mount technology used by the TempTouch® thermometer. Both display units employ solid-state displays, with the predicate using an LED display while the TempTouch thermometer uses an LCD display. ## Summary-Non-Clinical Performance Testing: | Performance Test | Results | |------------------------|---------| | Accuracy Test | Pass | | Repeatability Tests | Pass | | °F vs. °C tests | Pass | | Variable Voltage Tests | Pass | | Error Message Tests | Pass | | Display Limits Tests | Pass | Conclusion: Since performance testing confirms conformance to the same standard as the predicate device, we conclude the device is substantially equivalent to that device. {2}------------------------------------------------ Image /page/2/Picture/11 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a stylized eagle with its wings spread, and the text "DEPARTMENT OF HEALTH & HUMAN SERVICES . USA" is arranged in a circular fashion around the eagle. The eagle is black, and the text is also black. The background is white. Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 MAY - 8 2008 Diabetica Solutions Incorporated C/O Mr. Ned Devine Responsible Third Party Official Underwriters Laboratories, Incorporated 333 Pfingsten Road Northbrook, Illinois 60062 Re: K081162 Trade/Device Name: TempTouch® Regulation Number: 21 CFR 880.2910 Regulation Name: Clinical Electronic Thermometer Regulatory Class: II Product Code: FLL Dated: April 23, 2008 Received: April 24, 2008 Dear Mr. Devine: 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. {3}------------------------------------------------ ## Page 2 - Mr. Devine 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) 276-0115. 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 yours. Clive Shieh-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 {4}------------------------------------------------ ## STATEMENT OF INDICATIONS FOR USE 510(k) Number if known: __ Ko 8/163 Device Name: TempTouch® Indications for use: "The TempTouch® Dermal Thermometer is an infrared thermometer intended for the intermittent measurement of skin surface temperature of people of all ages." Prescription use: XX Part 21 CFR 801 Subpart D) AND/OR Over-The-Counter use: __ XX ___________________________________________________________________________________________________________________________________________________________________________ (21 CFR 807 Subpart C) (PLEASE DO NOT WRITE BELOW THIS LINE- CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) Page 1 of 1 Cinta air (Division Sign-Off) Division of Anesthesiology, General Hospital Infection Control, Dental Devices 510(k) Number: TempTouch® FDA Submission 27
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