OHIO THORACIC SUCTION REGULATOR— 510(k) K802285

Name: FDA 510(k) clearance K802285
Creator: U.S. Food and Drug Administration
Published: 1980-10-03

Substantially Equivalent

Ohio Medical Products

FDA 510(k) clearance K802285 for OHIO THORACIC SUCTION REGULATOR, Substantially Equivalent on 1980-10-03. Applicant: Ohio Medical Products. Device class: 1.

Clearance details

Applicant: Ohio Medical Products
Product code: Code KOP
Device class: Class 1
Regulation: 21 CFR 872.3450
Advisory panel: Dental
Date received: 1980-09-19
Decision date: 1980-10-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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