POST SURGICAL KIT/POST BIOPSY KIT— 510(k) K910011

Name: FDA 510(k) clearance K910011
Creator: U.S. Food and Drug Administration
Published: 1991-03-27

Substantially Equivalent

Dermatological Research Laboratories, Inc.

FDA 510(k) clearance K910011 for POST SURGICAL KIT/POST BIOPSY KIT, Substantially Equivalent on 1991-03-27. Applicant: Dermatological Research Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Dermatological Research Laboratories, Inc.
Product code: Code MCY
Device class: Class 2
Regulation: 21 CFR 880.5075
Advisory panel: General Hospital
Date received: 1991-01-02
Decision date: 1991-03-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Burlingame, CA, US

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