BBL ANAGEL POWDER— 510(k) K832229

Name: FDA 510(k) clearance K832229
Creator: U.S. Food and Drug Administration
Published: 1983-08-12

Substantially Equivalent

Bd Becton Dickinson Vacutainer Systems Preanalytic

FDA 510(k) clearance K832229 for BBL ANAGEL POWDER, Substantially Equivalent on 1983-08-12. Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic. Device class: 1.

Clearance details

Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic
Product code: Code KZJ
Device class: Class 1
Regulation: 21 CFR 866.2580
Advisory panel: Microbiology
Date received: 1983-07-11
Decision date: 1983-08-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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