FDA 510(k), K901449, VACUTAINER PLUS WITH HEMOGARD CLOSURE

FDA 510(k), K901449, VACUTAINER PLUS WITH HEMOGARD CLOSURE

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510(K) Number: K901449
Device Name: VACUTAINER PLUS WITH HEMOGARD CLOSURE
Manufacturer:
Device Classification Name: Tubes, Vials, Systems, Serum Separators, Blood Collection
Regulation Number: 862.1675
Classification Product Code: JKA
Date Received: 03/28/1990
Decision Date: 08/09/1990
Regulation Medical Specialty: Clinical Chemistry
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