FDA 510(k), K150059, BD FlowSmart Set

FDA 510(k), K150059, BD FlowSmart Set

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510(K) Number: K150059
Device Name: BD FlowSmart Set
Manufacturer: BECTON, DICKINSON COMPANY
Device Classification Name: set, administration, intravascular
Regulation Number: 880.5440
Classification Product Code: FPA
Date Received: 01/13/2015
Decision Date: 04/28/2015
Regulation Medical Specialty: General Hospital

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