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FDA 510(k)

FEVER TESTER

K-Number: K771980 · 1977-11-02

ApplicantAmerican Thermometer Company, Inc.
Decision Date1977-11-02
Product CodeKPD
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FEVER TESTER is the device name listed in this FDA 510(k) record. The listed applicant is American Thermometer Company, Inc.. It received FDA 510(k) clearance on 1977-11-02 under 510(k) number K771980. The device is classified under product code KPD. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FEVER TESTER?

FEVER TESTER is a medical device that received FDA 510(k) clearance on 1977-11-02. The listed applicant is American Thermometer Company, Inc.. The 510(k) number is K771980.

When did FEVER TESTER receive FDA 510(k) clearance?

FEVER TESTER received FDA 510(k) clearance on 1977-11-02, under 510(k) number K771980.

Who is the listed applicant for FEVER TESTER?

The FDA 510(k) record lists American Thermometer Company, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FEVER TESTER?

The FDA product code for FEVER TESTER is KPD.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing American Thermometer Company, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K823245THERMAX; THERMAX SYSTEMK821049PARATHERM

Related Devices (Code: KPD)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K934941E-Z TEMP IISeven C'S, Inc.K903307TEMP MARQ TEMPERATURE TREND INDICATORMarquest Medical Products, Inc.K893803FEVER LINE AND FEVER LINE PLUSLiquid Crystal Sciences, Inc.K864853OMNI THERM TEMPERATURE MONITOROmni Therm, Inc.K850797TEMPALERT LIQUID CRYSTAL THERMOMETERMedical Frontiers, Inc.K841913TEMPTREND PEDS AXILLARY TEMP. INDICATORBiosynergy, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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