AMMEX TUBING ORGANIZER— 510(k) K934782

Name: FDA 510(k) clearance K934782
Creator: U.S. Food and Drug Administration
Published: 1993-11-18

Substantially Equivalent

Ammex Cardiopulmonary Corp.

FDA 510(k) clearance K934782 for AMMEX TUBING ORGANIZER, Substantially Equivalent on 1993-11-18. Applicant: Ammex Cardiopulmonary Corp.. Device class: 1.

Clearance details

Applicant: Ammex Cardiopulmonary Corp.
Product code: Code KRI
Device class: Class 1
Regulation: 21 CFR 870.4200
Advisory panel: Cardiovascular
Date received: 1993-10-06
Decision date: 1993-11-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, US

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Data sourced from openFDA. This site is unofficial and independent of the FDA.