FDA 510(k), K903390, MEDRAD MARK V-PLUS INJECTOR

FDA 510(k), K903390, MEDRAD MARK V-PLUS INJECTOR

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510(K) Number: K903390
Device Name: MEDRAD MARK V-PLUS INJECTOR
Manufacturer:
Device Classification Name: Injector And Syringe, Angiographic
Regulation Number: 870.1650
Classification Product Code: DXT
Date Received: 07/27/1990
Decision Date: 09/26/1990
Regulation Medical Specialty: Cardiovascular
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