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FDA 510(k)

THE TOOTHPIK

K-Number: K830225 · 1983-02-18

ApplicantFred M. Davis
Decision Date1983-02-18
Product CodeJES
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

THE TOOTHPIK is the device name listed in this FDA 510(k) record. The listed applicant is Fred M. Davis. It received FDA 510(k) clearance on 1983-02-18 under 510(k) number K830225. The device is classified under product code JES. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE TOOTHPIK?

THE TOOTHPIK is a medical device that received FDA 510(k) clearance on 1983-02-18. The listed applicant is Fred M. Davis. The 510(k) number is K830225.

When did THE TOOTHPIK receive FDA 510(k) clearance?

THE TOOTHPIK received FDA 510(k) clearance on 1983-02-18, under 510(k) number K830225.

Who is the listed applicant for THE TOOTHPIK?

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

What is the FDA product code for THE TOOTHPIK?

The FDA product code for THE TOOTHPIK is JES.

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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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