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FDA 510(k)

TOMMY TOES

K-Number: K792331 · 1979-12-20

ApplicantTommy Toes
Decision Date1979-12-20
Product CodeFQM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TOMMY TOES is the device name listed in this FDA 510(k) record. The listed applicant is Tommy Toes. It received FDA 510(k) clearance on 1979-12-20 under 510(k) number K792331. The device is classified under product code FQM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOMMY TOES?

TOMMY TOES is a medical device that received FDA 510(k) clearance on 1979-12-20. The listed applicant is Tommy Toes. The 510(k) number is K792331.

When did TOMMY TOES receive FDA 510(k) clearance?

TOMMY TOES received FDA 510(k) clearance on 1979-12-20, under 510(k) number K792331.

Who is the listed applicant for TOMMY TOES?

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

What is the FDA product code for TOMMY TOES?

The FDA product code for TOMMY TOES is FQM.

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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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