MORGAN ARTHROSCOPIC MENESUS & SYNOVIAL RASP— 510(k) K853601

Name: FDA 510(k) clearance K853601
Creator: U.S. Food and Drug Administration
Published: 1985-09-16

Substantially Equivalent

Bowen & Company, Inc.

FDA 510(k) clearance K853601 for MORGAN ARTHROSCOPIC MENESUS & SYNOVIAL RASP, Substantially Equivalent on 1985-09-16. Applicant: Bowen & Company, Inc.. Device class: 1.

Clearance details

Applicant: Bowen & Company, Inc.
Product code: Code GAC
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1985-08-27
Decision date: 1985-09-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rockville, MD, US

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