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FDA 510(k), K991513, HOMEPUMP C-SERIES AND HOMEPUMP C-SERIES ONE-STEP KVO
FDA 510(k), K991513, HOMEPUMP C-SERIES AND HOMEPUMP C-SERIES ONE-STEP KVO
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510(K) Number: K991513
Device Name: HOMEPUMP C-SERIES AND HOMEPUMP C-SERIES ONE-STEP KVO
Manufacturer: I-FLOW CORP.
Device Classification Name: set, administration, intravascular
Regulation Number: 880.5440
Classification Product Code: FPA
Date Received: 04/30/1999
Decision Date: 06/21/1999
Regulation Medical Specialty: General Hospital
Device Name: HOMEPUMP C-SERIES AND HOMEPUMP C-SERIES ONE-STEP KVO
Manufacturer: I-FLOW CORP.
Device Classification Name: set, administration, intravascular
Regulation Number: 880.5440
Classification Product Code: FPA
Date Received: 04/30/1999
Decision Date: 06/21/1999
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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