VALVE, I.M.V. (U-MID ONE WAY)— 510(k) K760039

Name: FDA 510(k) clearance K760039
Creator: U.S. Food and Drug Administration
Published: 1976-07-16

Substantially Equivalent

Bd Becton Dickinson Vacutainer Systems Preanalytic

FDA 510(k) clearance K760039 for VALVE, I.M.V. (U-MID ONE WAY), Substantially Equivalent on 1976-07-16. Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic. Device class: 2.

Clearance details

Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic
Product code: Code CBO
Device class: Class 2
Regulation: 21 CFR 868.5955
Advisory panel: Anesthesiology
Date received: 1976-06-15
Decision date: 1976-07-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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