SURGICAL INSTRUMENT GUIDE— 510(k) K950007

Name: FDA 510(k) clearance K950007
Creator: U.S. Food and Drug Administration
Published: 1995-03-15

Substantially Equivalent

United States Surgical, A Division of Tyco Healthc

FDA 510(k) clearance K950007 for SURGICAL INSTRUMENT GUIDE, Substantially Equivalent on 1995-03-15. Applicant: United States Surgical, A Division of Tyco Healthc. Device class: 1.

Clearance details

Applicant: United States Surgical, A Division of Tyco Healthc
Product code: Code GDF
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1995-01-03
Decision date: 1995-03-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norwalk, CT, US

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