STERILE BANDAGE, GAUZE, FINE MESH, 3X8 INCHES— 510(k) K914937

Name: FDA 510(k) clearance K914937
Creator: U.S. Food and Drug Administration
Published: 1991-12-04

Substantially Equivalent

Kerma Medical Products, Inc.

FDA 510(k) clearance K914937 for STERILE BANDAGE, GAUZE, FINE MESH, 3X8 INCHES, Substantially Equivalent on 1991-12-04. Applicant: Kerma Medical Products, Inc.. Device class: 1.

Clearance details

Applicant: Kerma Medical Products, Inc.
Product code: Code NAB
Device class: Class 1
Regulation: 21 CFR 878.4014
Advisory panel: General, Plastic Surgery
Date received: 1991-11-04
Decision date: 1991-12-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chesapeake, VA, US

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