FIBROSYSTEM— 510(k) K823520

Name: FDA 510(k) clearance K823520
Creator: U.S. Food and Drug Administration
Published: 1982-12-28

Substantially Equivalent

Bd Becton Dickinson Vacutainer Systems Preanalytic

FDA 510(k) clearance K823520 for FIBROSYSTEM, Substantially Equivalent on 1982-12-28. Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic. Device class: 1.

Clearance details

Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic
Product code: Code GKQ
Device class: Class 1
Regulation: 21 CFR 864.7900
Advisory panel: Hematology
Date received: 1982-11-29
Decision date: 1982-12-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

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