BARD-PARKER ARTERIAL MONITORING SYSTEM— 510(k) K780939

Name: FDA 510(k) clearance K780939
Creator: U.S. Food and Drug Administration
Published: 1978-07-17

Substantially Equivalent

Bd Becton Dickinson Vacutainer Systems Preanalytic

FDA 510(k) clearance K780939 for BARD-PARKER ARTERIAL MONITORING SYSTEM, Substantially Equivalent on 1978-07-17. Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic. Device class: 1.

Clearance details

Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic
Product code: Code CBT
Device class: Class 1
Regulation: 21 CFR 868.1100
Advisory panel: Anesthesiology
Date received: 1978-06-08
Decision date: 1978-07-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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