OHIO DISPOSABLE CLEAR SUCTION INSTRUMENT— 510(k) K801641

Name: FDA 510(k) clearance K801641
Creator: U.S. Food and Drug Administration
Published: 1980-07-28

Substantially Equivalent

Ohio Medical Products

FDA 510(k) clearance K801641 for OHIO DISPOSABLE CLEAR SUCTION INSTRUMENT, Substantially Equivalent on 1980-07-28. Applicant: Ohio Medical Products. Device class: 2.

Clearance details

Applicant: Ohio Medical Products
Product code: Code DTS
Device class: Class 2
Regulation: 21 CFR 870.4420
Advisory panel: Cardiovascular
Date received: 1980-07-17
Decision date: 1980-07-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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