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FDA 510(k)

FOLEY INSERTION TRAYS W/OVERWRAY

K-Number: K820987 · 1982-05-13

ApplicantInmed Corp.
Decision Date1982-05-13
Product CodeKOD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FOLEY INSERTION TRAYS W/OVERWRAY is the device name listed in this FDA 510(k) record. The listed applicant is Inmed Corp.. It received FDA 510(k) clearance on 1982-05-13 under 510(k) number K820987. The device is classified under product code KOD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FOLEY INSERTION TRAYS W/OVERWRAY?

FOLEY INSERTION TRAYS W/OVERWRAY is a medical device that received FDA 510(k) clearance on 1982-05-13. The listed applicant is Inmed Corp.. The 510(k) number is K820987.

When did FOLEY INSERTION TRAYS W/OVERWRAY receive FDA 510(k) clearance?

FOLEY INSERTION TRAYS W/OVERWRAY received FDA 510(k) clearance on 1982-05-13, under 510(k) number K820987.

Who is the listed applicant for FOLEY INSERTION TRAYS W/OVERWRAY?

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

What is the FDA product code for FOLEY INSERTION TRAYS W/OVERWRAY?

The FDA product code for FOLEY INSERTION TRAYS W/OVERWRAY is KOD.

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Related Devices (Code: KOD)

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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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