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FDA 510(k)

MODEL F-1010 DIGITAL THERMOMETER

K-Number: K791371 · 1979-09-17

ApplicantFilac Corp.
Decision Date1979-09-17
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODEL F-1010 DIGITAL THERMOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Filac Corp.. It received FDA 510(k) clearance on 1979-09-17 under 510(k) number K791371. 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 MODEL F-1010 DIGITAL THERMOMETER?

MODEL F-1010 DIGITAL THERMOMETER is a medical device that received FDA 510(k) clearance on 1979-09-17. The listed applicant is Filac Corp.. The 510(k) number is K791371.

When did MODEL F-1010 DIGITAL THERMOMETER receive FDA 510(k) clearance?

MODEL F-1010 DIGITAL THERMOMETER received FDA 510(k) clearance on 1979-09-17, under 510(k) number K791371.

Who is the listed applicant for MODEL F-1010 DIGITAL THERMOMETER?

The FDA 510(k) record lists Filac Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL F-1010 DIGITAL THERMOMETER?

The FDA product code for MODEL F-1010 DIGITAL 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

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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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