DESERET ARTERIAL BLOOD SAMPLING KIT— 510(k) K822248

Name: FDA 510(k) clearance K822248
Creator: U.S. Food and Drug Administration
Published: 1982-10-21

Substantially Equivalent

Warner-Lambert Co.

FDA 510(k) clearance K822248 for DESERET ARTERIAL BLOOD SAMPLING KIT, Substantially Equivalent on 1982-10-21. Applicant: Warner-Lambert Co.. Device class: 1.

Clearance details

Applicant: Warner-Lambert Co.
Product code: Code CBT
Device class: Class 1
Regulation: 21 CFR 868.1100
Advisory panel: Anesthesiology
Date received: 1982-07-29
Decision date: 1982-10-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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