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
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
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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