ARD(TM) ANTIMICROBIAL REMOVAL DEVICE— 510(k) K911771

Name: FDA 510(k) clearance K911771
Creator: U.S. Food and Drug Administration
Published: 1991-07-01

Substantially Equivalent

Bd Becton Dickinson Vacutainer Systems Preanalytic

FDA 510(k) clearance K911771 for ARD(TM) ANTIMICROBIAL REMOVAL DEVICE, Substantially Equivalent on 1991-07-01. Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic. Device class: 2.

Clearance details

Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic
Product code: Code LJK
Device class: Class 2
Regulation: 21 CFR 866.3780
Advisory panel: Microbiology
Date received: 1991-04-19
Decision date: 1991-07-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Franklin Lakes, NJ, US

Download summary PDF View on FDA.gov ↗

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