CRITIKON TRANSCUTANEOUS GAS MONITORS— 510(k) K813347

Name: FDA 510(k) clearance K813347
Creator: U.S. Food and Drug Administration
Published: 1982-01-26

Substantially Equivalent

Critikon Company, LLC

FDA 510(k) clearance K813347 for CRITIKON TRANSCUTANEOUS GAS MONITORS, Substantially Equivalent on 1982-01-26. Applicant: Critikon Company, LLC. Device class: 2.

Clearance details

Applicant: Critikon Company, LLC
Product code: Code KLK
Device class: Class 2
Regulation: 21 CFR 868.2500
Advisory panel: Anesthesiology
Date received: 1981-11-27
Decision date: 1982-01-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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