← Product Code [FLL](/submissions/HO/subpart-c%E2%80%94general-hospital-and-personal-use-monitoring-devices/FLL) · K052849 # INFRARED THERMOMETER, FDIR-V1 (K052849) _Famidoc Technology Co., Ltd. · FLL · Oct 26, 2005 · General Hospital · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/HO/subpart-c%E2%80%94general-hospital-and-personal-use-monitoring-devices/FLL/K052849 ## Device Facts - **Applicant:** Famidoc Technology Co., Ltd. - **Product Code:** [FLL](/submissions/HO/subpart-c%E2%80%94general-hospital-and-personal-use-monitoring-devices/FLL.md) - **Decision Date:** Oct 26, 2005 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 880.2910 - **Device Class:** Class 2 - **Review Panel:** General Hospital - **Attributes:** 3rd-Party Reviewed ## Indications for Use Model: FDIR-V1 is intended for the Thermometer Infrared intermittent measurement and monitoring of human body temperature, by consumers in the home. ## Device Story Hand-held, battery-operated infrared thermometer; measures human body temperature via forehead skin or tympanic (ear) canal. Principle of operation: infrared sensor detects thermal radiation; ASIC converts sensor signal to digital value; LCD displays temperature. Used by consumers in home environment. Provides non-invasive temperature readings to assist in monitoring health status. ## Clinical Evidence Bench testing only. Device conforms to ASTM E1965-98, EN 12470-5: 2003, IEC 60601-1, and IEC 60601-1-2 standards. ## Technological Characteristics Infrared sensor technology; ASIC-based signal processing; LCD display; battery-operated; hand-held form factor. Conforms to ASTM E1965-98, EN 12470-5: 2003, IEC 60601-1, and IEC 60601-1-2. ## Regulatory 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 - AVITA TS8 Series IR Ear/Forehead Thermometer ([K031503](/device/K031503.md)) ## Submission Summary (Full Text) > This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com. > > Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/). {0}------------------------------------------------ OCT 26 2005 K052849 (f. 1 of 2) ## 510(K) SUMMARY This summary of 510(k) safety and effectiveness information is being submitted in accordance with the requirements of SMDA and 21 CFR § 807.92 | 1.0 Submitter's Name: | FAMIDOC TECHNOLOGY CO., LTD. | |-----------------------|---------------------------------------------------------------------------------| | Address: | 3rd Floor, East Block4, Chegongmiao Anhua
Industrial Zone Shenzhen P.R.China | | Phone: | +86-755-83412736 | | Fax: | +86-755-83429513 | | Contact: | Mr. Steeljin, | | E-mail: | steeljin@famidoc.com
Jason@famidoc.com | | 2.0 Device Name: | Infrared Thermometer | |----------------------|---------------------------------| | | Model: FDIR-V1 | | Classification Name: | Clinical Electronic Thermometer | - 3.0 Classification: Class N 4.0 Predicate Device Information: AVITA TS8 Series IR Ear/Forehead Thermometer. Model NO.: TS-802 3 in 1 Ear/Forehead/Room Thermometer for the TS8 Series. It's 510(k) number is K031503. #### 5.0 Device Description: Infrared Thermometer Model: FDIR-VI is a hand-held, reusable, battery operated, maximum device that can measures human body temperature by two ways. 1. on forehead, the skin temperature on one's forehead. 2. in ear, the tympanic temperature in one's ear. The operation principle is based on Infrared Sensor technology. IR Sensor can putout different signal when measuring different object temperature or in different ambient temperature, an ASIC can turn the {1}------------------------------------------------ signal from IR Sensor to a digital value and display it by LCD. ### 6.0 Intended Use: Model: FDIR-V1 is intended for the Thermometer Infrared intermittent measurement and monitoring of human body temperature, by consumers in the home. ## 7.0 Performance Summary The device conforms to applicable standards included ASTM E1965-98, EN 12470-5: 2003, IEC 60601-1 and IEC 60601-1-2 requirements. ## 8.0 Comparison to Predicate Devices and conclusions Our Infrared Thermometer Model FDIR-V1 is substantially equivalent to AVITA 3 in 1 Ear/Forehead/Room Thermometer for the TS8 Series Model TS-802, It's 510(k) number is K031503. The two device are very similar in design principle, intended use, functions, material and the adopting applicable standards. Only their outlook and some parameter such as measurement range, battery life are different. moreover, tests in this submission provide demonstrate these small difference do not raise and new questions of safety or effectiveness. Conclusions: the Infrared Thermometer Model FDIR-V1 is substantially equivalent to the predicate devices. {2}------------------------------------------------ DEPARTMENT OF HEALTH & HUMAN SERVICES Image /page/2/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a stylized caduceus symbol, which features a staff with a serpent entwined around it, and three horizontal bars above it. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" is arranged in a circular fashion around the symbol. Public Health Service OCT 2 6 2005 Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 Famidoc Technology Company, Limited C/O Mr. Marc M. Mouser Responsible Third Party Official Underwriters Laboratories, Incorporated Laboratory and Testing 2600 NW Lake Road Camas, Washington 98607-8542 Re: K052849 Trade/Device Name: INFRARED THERMOMETER, FDIR-VI Regulation Number: 21 CFR 880.2910 Regulation Name: Clinical Electronic Thermometer Regulatory Class: II Product Code: FLL Dated: September 5, 2005 Received: October 11, 2005 Dear Mr. Mouser: We have reviewed your Section 510(k) premarket notification of intent to market the device we nave roviewed your betermined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate for use stated in the encreatinent date of the enactment date of the Medical Device Amendments, or to conimered proz to they 2011 11:25 accordance with the provisions of the Federal Food, Drug, de vices that have been require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The r ou may, dierelore, mains of the Act include requirements for annual registration, listing of general controls provisioning practice, labeling, and prohibitions against misbranding and adulteration. If your device is classified (see above) into cither class II (Special Controls) or class III (PMA), it 11 your de vice is elabilities (tional controls. Existing major regulations affecting your device can may be subject to sueritadors. Title 21, Parts 800 to 898. In addition, FDA may be found in the obas acements concerning your device in the Federal Register. {3}------------------------------------------------ #### Page 2 - Mr. Mouser 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 erth 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 other generals, 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. Sincercly yours, 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}------------------------------------------------ # Indications for Use Ψ52849 510(k) Number (if known): Device Name: Infrared Thermometer Indications for Use: The device is intended for the intermittent measurement and monitoring of human body temperature, by consumers in the home. Prescription Use _____________________________________________________________________________________________________________________________________________________________ (Part 21 CFR 801 Subpart D) AND/OR Over-The-Counter Use (21 CFR 807 Subpart C) のお気になると、それでは、それは、それは、この時には、この時には、この時には、この時に、この時に se \$\times\$ C) (PLEASE DO NOT WRITE: BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) Cinta Dm Sien-City tion of Anas Instology, Ganeral Hospital, cilon Control, Demal Devices ______________________________________________________________________________________________________________________________________________________________________________ Page 1 of 1 719(k) Number _ K45284 9 --- **Source:** [https://fda.innolitics.com/submissions/HO/subpart-c%E2%80%94general-hospital-and-personal-use-monitoring-devices/FLL/K052849](https://fda.innolitics.com/submissions/HO/subpart-c%E2%80%94general-hospital-and-personal-use-monitoring-devices/FLL/K052849) **Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. 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