LEUCOPREP BRAND TUBE— 510(k) K872775

Name: FDA 510(k) clearance K872775
Creator: U.S. Food and Drug Administration
Published: 1987-10-02

Substantially Equivalent

Bd Becton Dickinson Vacutainer Systems Preanalytic

FDA 510(k) clearance K872775 for LEUCOPREP BRAND TUBE, Substantially Equivalent on 1987-10-02. Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic. Device class: 1.

Clearance details

Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic
Product code: Code JCF
Device class: Class 1
Regulation: 21 CFR 864.8500
Advisory panel: Hematology
Date received: 1987-07-14
Decision date: 1987-10-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Franklin Lakes, NJ, US

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