KAY-MED SURGICAL DEAPE/DRAP ACCESSORIES— 510(k) K914761

Name: FDA 510(k) clearance K914761
Creator: U.S. Food and Drug Administration
Published: 1992-04-06

Substantially Equivalent

Kayco Medical, Inc.

FDA 510(k) clearance K914761 for KAY-MED SURGICAL DEAPE/DRAP ACCESSORIES, Substantially Equivalent on 1992-04-06. Applicant: Kayco Medical, Inc.. Device class: 2.

Clearance details

Applicant: Kayco Medical, Inc.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1991-10-22
Decision date: 1992-04-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chicago, IL, US

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