FDA 510(k), K984146, PARAGON INFUSION
FDA 510(k), K984146, PARAGON INFUSION
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510(K) Number: K984146
Device Name: PARAGON INFUSION
Manufacturer:
Device Classification Name: Set, Administration, Intravascular
Regulation Number: 880.5440
Classification Product Code: FPA
Date Received: 11/19/1998
Decision Date: 02/09/1999
Regulation Medical Specialty: General Hospital
Device Name: PARAGON INFUSION
Manufacturer:
Device Classification Name: Set, Administration, Intravascular
Regulation Number: 880.5440
Classification Product Code: FPA
Date Received: 11/19/1998
Decision Date: 02/09/1999
Regulation Medical Specialty: General Hospital