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FDA 510(k), K101677, HOSPIRA INFUSION BLOOD SETS
FDA 510(k), K101677, HOSPIRA INFUSION BLOOD SETS
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510(K) Number: K101677
Device Name: HOSPIRA INFUSION BLOOD SETS
Manufacturer: HOSPIRA, INC.
Device Classification Name: set, administration, intravascular
Regulation Number: 880.5440
Classification Product Code: FPA
Date Received: 06/15/2010
Decision Date: 08/11/2010
Regulation Medical Specialty: General Hospital
Device Name: HOSPIRA INFUSION BLOOD SETS
Manufacturer: HOSPIRA, INC.
Device Classification Name: set, administration, intravascular
Regulation Number: 880.5440
Classification Product Code: FPA
Date Received: 06/15/2010
Decision Date: 08/11/2010
Regulation Medical Specialty: General Hospital
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- 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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