AUTOSCEPTOR IDENTIFICATION SYSTEM— 510(k) K920225

Name: FDA 510(k) clearance K920225
Creator: U.S. Food and Drug Administration
Published: 1992-05-22

Substantially Equivalent

Bd Becton Dickinson Vacutainer Systems Preanalytic

FDA 510(k) clearance K920225 for AUTOSCEPTOR IDENTIFICATION SYSTEM, Substantially Equivalent on 1992-05-22. Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic. Device class: 1.

Clearance details

Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic
Product code: Code LRH
Device class: Class 1
Regulation: 21 CFR 866.2660
Advisory panel: Microbiology
Date received: 1992-01-17
Decision date: 1992-05-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Franklin Lakes, NJ, US

Download summary PDF View on FDA.gov ↗

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