PULSATOR ARTERIAL BLOOD SAMPLING SYRIN— 510(k) K833582

Name: FDA 510(k) clearance K833582
Creator: U.S. Food and Drug Administration
Published: 1983-12-27

Substantially Equivalent

Concord Laboratories, Inc.

FDA 510(k) clearance K833582 for PULSATOR ARTERIAL BLOOD SAMPLING SYRIN, Substantially Equivalent on 1983-12-27. Applicant: Concord Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Concord Laboratories, Inc.
Product code: Code CBT
Device class: Class 1
Regulation: 21 CFR 868.1100
Advisory panel: Anesthesiology
Date received: 1983-10-12
Decision date: 1983-12-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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