ARTAP ARTERIAL BLOOD SAMPLING DEVICE— 510(k) K843360

Name: FDA 510(k) clearance K843360
Creator: U.S. Food and Drug Administration
Published: 1984-10-31

Substantially Equivalent

Analytical Products, Inc.

FDA 510(k) clearance K843360 for ARTAP ARTERIAL BLOOD SAMPLING DEVICE, Substantially Equivalent on 1984-10-31. Applicant: Analytical Products, Inc.. Device class: 1.

Clearance details

Applicant: Analytical Products, Inc.
Product code: Code CBT
Device class: Class 1
Regulation: 21 CFR 868.1100
Advisory panel: Anesthesiology
Date received: 1984-08-28
Decision date: 1984-10-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Belmont, CA, US

Download summary PDF View on FDA.gov ↗

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