OHMEDA CONTINUOUS SUCTION REGULATOR— 510(k) K883229

Name: FDA 510(k) clearance K883229
Creator: U.S. Food and Drug Administration
Published: 1988-10-19

Substantially Equivalent

Ohmeda Medical

FDA 510(k) clearance K883229 for OHMEDA CONTINUOUS SUCTION REGULATOR, Substantially Equivalent on 1988-10-19. Applicant: Ohmeda Medical. Device class: 2.

Clearance details

Applicant: Ohmeda Medical
Product code: Code KDP
Device class: Class 2
Regulation: 21 CFR 880.6740
Advisory panel: General Hospital
Date received: 1988-08-01
Decision date: 1988-10-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Columbia, MD, US

Download summary PDF View on FDA.gov ↗

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