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FDA 510(k)

MEDI-THERM SKIN THERMOMETER

K-Number: K822435 · 1982-09-22

Decision Date1982-09-22
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEDI-THERM SKIN THERMOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Everest Interscience, Inc.. It received FDA 510(k) clearance on 1982-09-22 under 510(k) number K822435. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDI-THERM SKIN THERMOMETER?

MEDI-THERM SKIN THERMOMETER is a medical device that received FDA 510(k) clearance on 1982-09-22. The listed applicant is Everest Interscience, Inc.. The 510(k) number is K822435.

When did MEDI-THERM SKIN THERMOMETER receive FDA 510(k) clearance?

MEDI-THERM SKIN THERMOMETER received FDA 510(k) clearance on 1982-09-22, under 510(k) number K822435.

Who is the listed applicant for MEDI-THERM SKIN THERMOMETER?

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

What is the FDA product code for MEDI-THERM SKIN THERMOMETER?

The FDA product code for MEDI-THERM SKIN THERMOMETER is FLL.

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: FLL)

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

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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