MEDICAL PROCEDURE KITS/ARTERIAL BLOOD SAMPLING— 510(k) K905464

Name: FDA 510(k) clearance K905464
Creator: U.S. Food and Drug Administration
Published: 1991-05-31

Unknown

Angiosystems, Inc.

FDA 510(k) clearance K905464 for MEDICAL PROCEDURE KITS/ARTERIAL BLOOD SAMPLING, Unknown on 1991-05-31. Applicant: Angiosystems, Inc.. Device class: 1.

Clearance details

Applicant: Angiosystems, Inc.
Product code: Code CBT
Device class: Class 1
Regulation: 21 CFR 868.1100
Advisory panel: Anesthesiology
Date received: 1990-12-05
Decision date: 1991-05-31
Decision: Unknown
Clearance type: Traditional
Location: Great Neck, NY, US

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