TRANSCUTANEOUS OXYGEN MONITOR OPTION— 510(k) K831744

Name: FDA 510(k) clearance K831744
Creator: U.S. Food and Drug Administration
Published: 1983-07-19

Substantially Equivalent

Ge Medical Systems Information Technologies

FDA 510(k) clearance K831744 for TRANSCUTANEOUS OXYGEN MONITOR OPTION, Substantially Equivalent on 1983-07-19. Applicant: Ge Medical Systems Information Technologies. Device class: 2.

Clearance details

Applicant: Ge Medical Systems Information Technologies
Product code: Code KLK
Device class: Class 2
Regulation: 21 CFR 868.2500
Advisory panel: Anesthesiology
Date received: 1983-05-31
Decision date: 1983-07-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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