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FDA 510(k)

TEMPALERT LIQUID CRYSTAL THERMOMETER

K-Number: K850797 · 1985-04-05

Decision Date1985-04-05
Product CodeKPD
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TEMPALERT LIQUID CRYSTAL THERMOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Medical Frontiers, Inc.. It received FDA 510(k) clearance on 1985-04-05 under 510(k) number K850797. 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 TEMPALERT LIQUID CRYSTAL THERMOMETER?

TEMPALERT LIQUID CRYSTAL THERMOMETER is a medical device that received FDA 510(k) clearance on 1985-04-05. The listed applicant is Medical Frontiers, Inc.. The 510(k) number is K850797.

When did TEMPALERT LIQUID CRYSTAL THERMOMETER receive FDA 510(k) clearance?

TEMPALERT LIQUID CRYSTAL THERMOMETER received FDA 510(k) clearance on 1985-04-05, under 510(k) number K850797.

Who is the listed applicant for TEMPALERT LIQUID CRYSTAL THERMOMETER?

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

What is the FDA product code for TEMPALERT LIQUID CRYSTAL THERMOMETER?

The FDA product code for TEMPALERT LIQUID CRYSTAL THERMOMETER 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.

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.

Official Source

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

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