FDA 510(k)

CHEEK TOOL SET

K-Number: K802138 · 1980-10-31

Decision Date1980-10-31

Product CodeGWM

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

CHEEK TOOL SET is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 1980-10-31 under 510(k) number K802138. The device is classified under product code GWM. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHEEK TOOL SET?

CHEEK TOOL SET is a medical device that received FDA 510(k) clearance on 1980-10-31. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K802138.

When did CHEEK TOOL SET receive FDA 510(k) clearance?

CHEEK TOOL SET received FDA 510(k) clearance on 1980-10-31, under 510(k) number K802138.

Who is the listed applicant for CHEEK TOOL SET?

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

What is the FDA product code for CHEEK TOOL SET?

The FDA product code for CHEEK TOOL SET is GWM.

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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.