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FDA 510(k)

PAD, POLYETHER FOAM, OPEN CELL

K-Number: K760315 · 1976-08-11

ApplicantGaymar Industries, Inc.
Decision Date1976-08-11
Product CodeFNJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PAD, POLYETHER FOAM, OPEN CELL is the device name listed in this FDA 510(k) record. The listed applicant is Gaymar Industries, Inc.. It received FDA 510(k) clearance on 1976-08-11 under 510(k) number K760315. The device is classified under product code FNJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PAD, POLYETHER FOAM, OPEN CELL?

PAD, POLYETHER FOAM, OPEN CELL is a medical device that received FDA 510(k) clearance on 1976-08-11. The listed applicant is Gaymar Industries, Inc.. The 510(k) number is K760315.

When did PAD, POLYETHER FOAM, OPEN CELL receive FDA 510(k) clearance?

PAD, POLYETHER FOAM, OPEN CELL received FDA 510(k) clearance on 1976-08-11, under 510(k) number K760315.

Who is the listed applicant for PAD, POLYETHER FOAM, OPEN CELL?

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

What is the FDA product code for PAD, POLYETHER FOAM, OPEN CELL?

The FDA product code for PAD, POLYETHER FOAM, OPEN CELL is FNJ.

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Related Devices (Code: FNJ)

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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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