ACROMED WALLIE-HEINIG DISECTOR/ELEVATORS— 510(k) K870781

Name: FDA 510(k) clearance K870781
Creator: U.S. Food and Drug Administration
Published: 1987-03-09

Substantially Equivalent

Buckman Co., Inc.

FDA 510(k) clearance K870781 for ACROMED WALLIE-HEINIG DISECTOR/ELEVATORS, Substantially Equivalent on 1987-03-09. Applicant: Buckman Co., Inc.. Device class: 1.

Clearance details

Applicant: Buckman Co., Inc.
Product code: Code GEG
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1987-02-26
Decision date: 1987-03-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Martinez, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.