PRECISION GLIDE - ENHANCED SURGICAL BLADE— 510(k) K911913

Name: FDA 510(k) clearance K911913
Creator: U.S. Food and Drug Administration
Published: 1991-05-13

Substantially Equivalent

Bd Becton Dickinson Vacutainer Systems Preanalytic

FDA 510(k) clearance K911913 for PRECISION GLIDE - ENHANCED SURGICAL BLADE, Substantially Equivalent on 1991-05-13. Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic. Device class: 1.

Clearance details

Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic
Product code: Code GES
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1991-04-30
Decision date: 1991-05-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Franklin Lakes, NJ, US

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