B-D DRAKE WILLOCK #7000 SERIES ULTRAF— 510(k) K811591

Name: FDA 510(k) clearance K811591
Creator: U.S. Food and Drug Administration
Published: 1981-07-10

Substantially Equivalent

Bd Becton Dickinson Vacutainer Systems Preanalytic

FDA 510(k) clearance K811591 for B-D DRAKE WILLOCK #7000 SERIES ULTRAF, Substantially Equivalent on 1981-07-10. Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic. Device class: 2.

Clearance details

Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic
Product code: Code FKP
Device class: Class 2
Regulation: 21 CFR 876.5820
Advisory panel: Gastroenterology, Urology
Date received: 1981-06-08
Decision date: 1981-07-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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