OXY MONITOR 5-RANGE DUAL-THERMISTOR— 510(k) K832652

Name: FDA 510(k) clearance K832652
Creator: U.S. Food and Drug Administration
Published: 1983-12-22

Substantially Equivalent

Litton Medical Electronics

FDA 510(k) clearance K832652 for OXY MONITOR 5-RANGE DUAL-THERMISTOR, Substantially Equivalent on 1983-12-22. Applicant: Litton Medical Electronics. Device class: 2.

Clearance details

Applicant: Litton Medical Electronics
Product code: Code KLK
Device class: Class 2
Regulation: 21 CFR 868.2500
Advisory panel: Anesthesiology
Date received: 1983-08-08
Decision date: 1983-12-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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