FDA 510(k), K964853, INTRAVIA CONTAINER, EMPTY
FDA 510(k), K964853, INTRAVIA CONTAINER, EMPTY
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510(K) Number: K964853
Device Name: INTRAVIA CONTAINER, EMPTY
Manufacturer:
Device Classification Name: Container, I.V.
Regulation Number: 880.5025
Classification Product Code: KPE
Date Received: 12/03/1996
Decision Date: 03/31/1997
Regulation Medical Specialty: General Hospital
Device Name: INTRAVIA CONTAINER, EMPTY
Manufacturer:
Device Classification Name: Container, I.V.
Regulation Number: 880.5025
Classification Product Code: KPE
Date Received: 12/03/1996
Decision Date: 03/31/1997
Regulation Medical Specialty: General Hospital