PRINCETON BIOMEDIX URICASE (UV)— 510(k) K780859

Name: FDA 510(k) clearance K780859
Creator: U.S. Food and Drug Administration
Published: 1978-07-27

Substantially Equivalent

Bd Becton Dickinson Vacutainer Systems Preanalytic

FDA 510(k) clearance K780859 for PRINCETON BIOMEDIX URICASE (UV), Substantially Equivalent on 1978-07-27. Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic. Device class: 1.

Clearance details

Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic
Product code: Code CDO
Device class: Class 1
Regulation: 21 CFR 862.1775
Advisory panel: Clinical Chemistry
Date received: 1978-05-24
Decision date: 1978-07-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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