DIFFUSION OPTION, OMNI-LAB— 510(k) K781871

Name: FDA 510(k) clearance K781871
Creator: U.S. Food and Drug Administration
Published: 1979-01-02

Substantially Equivalent

Ohio Medical Products

FDA 510(k) clearance K781871 for DIFFUSION OPTION, OMNI-LAB, Substantially Equivalent on 1979-01-02. Applicant: Ohio Medical Products. Device class: 2.

Clearance details

Applicant: Ohio Medical Products
Product code: Code CCJ
Device class: Class 2
Regulation: 21 CFR 868.1430
Advisory panel: Anesthesiology
Date received: 1978-11-03
Decision date: 1979-01-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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