BLOOD LEVEL DETECTOR-MODEL 7601— 510(k) K781330

Name: FDA 510(k) clearance K781330
Creator: U.S. Food and Drug Administration
Published: 1978-08-31

Substantially Equivalent

Bd Becton Dickinson Vacutainer Systems Preanalytic

FDA 510(k) clearance K781330 for BLOOD LEVEL DETECTOR-MODEL 7601, Substantially Equivalent on 1978-08-31. Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic. Device class: 2.

Clearance details

Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic
Product code: Code FJF
Device class: Class 2
Regulation: 21 CFR 876.5820
Advisory panel: Gastroenterology, Urology
Date received: 1978-08-02
Decision date: 1978-08-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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