DYNACYT BIOPSY ASPIRATION DEVICE— 510(k) K922919

Name: FDA 510(k) clearance K922919
Creator: U.S. Food and Drug Administration
Published: 1993-03-31

Substantially Equivalent

Buckman Co., Inc.

FDA 510(k) clearance K922919 for DYNACYT BIOPSY ASPIRATION DEVICE, Substantially Equivalent on 1993-03-31. Applicant: Buckman Co., Inc.. Device class: 1.

Clearance details

Applicant: Buckman Co., Inc.
Product code: Code MJG
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1992-06-17
Decision date: 1993-03-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Concord, CA, US

Download summary PDF View on FDA.gov ↗

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