IL 301 TRANSCUTANEOUS OXYGEN MONITOR— 510(k) K822328

Name: FDA 510(k) clearance K822328
Creator: U.S. Food and Drug Administration
Published: 1982-09-07

Substantially Equivalent

Instrumentation Laboratory CO

FDA 510(k) clearance K822328 for IL 301 TRANSCUTANEOUS OXYGEN MONITOR, Substantially Equivalent on 1982-09-07. Applicant: Instrumentation Laboratory CO. Device class: 2.

Clearance details

Applicant: Instrumentation Laboratory CO
Product code: Code KLK
Device class: Class 2
Regulation: 21 CFR 868.2500
Advisory panel: Anesthesiology
Date received: 1982-08-03
Decision date: 1982-09-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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