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FDA 510(k)

KAY-MED SURGICAL DEAPE/DRAP ACCESSORIES

K-Number: K914761 · 1992-04-06

ApplicantKayco Medical, Inc.
Decision Date1992-04-06
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KAY-MED SURGICAL DEAPE/DRAP ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Kayco Medical, Inc.. It received FDA 510(k) clearance on 1992-04-06 under 510(k) number K914761. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KAY-MED SURGICAL DEAPE/DRAP ACCESSORIES?

KAY-MED SURGICAL DEAPE/DRAP ACCESSORIES is a medical device that received FDA 510(k) clearance on 1992-04-06. The listed applicant is Kayco Medical, Inc.. The 510(k) number is K914761.

When did KAY-MED SURGICAL DEAPE/DRAP ACCESSORIES receive FDA 510(k) clearance?

KAY-MED SURGICAL DEAPE/DRAP ACCESSORIES received FDA 510(k) clearance on 1992-04-06, under 510(k) number K914761.

Who is the listed applicant for KAY-MED SURGICAL DEAPE/DRAP ACCESSORIES?

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

What is the FDA product code for KAY-MED SURGICAL DEAPE/DRAP ACCESSORIES?

The FDA product code for KAY-MED SURGICAL DEAPE/DRAP ACCESSORIES is KKX.

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Related Devices (Code: KKX)

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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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