HEM-O-SCAN OXYGEN EQUIL. CURVE ANALYZER— 510(k) K802379

Name: FDA 510(k) clearance K802379
Creator: U.S. Food and Drug Administration
Published: 1980-10-31

Substantially Equivalent

American Instrument Co.

FDA 510(k) clearance K802379 for HEM-O-SCAN OXYGEN EQUIL. CURVE ANALYZER, Substantially Equivalent on 1980-10-31. Applicant: American Instrument Co.. Device class: 1.

Clearance details

Applicant: American Instrument Co.
Product code: Code LCH
Device class: Class 1
Regulation: 21 CFR 862.1660
Advisory panel: Clinical Chemistry
Date received: 1980-09-30
Decision date: 1980-10-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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