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FDA 510(k), K051568, CADD-MS 3 AMBULATORY INFUSION PUMP
FDA 510(k), K051568, CADD-MS 3 AMBULATORY INFUSION PUMP
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510(K) Number: K051568
Device Name: CADD-MS 3 AMBULATORY INFUSION PUMP
Manufacturer: MELANIE HESS
Device Classification Name: Pump, Infusion
Regulation Number: FRN
Classification Product Code: 06/14/2005
Date Received: 11/17/2005
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: CADD-MS 3 AMBULATORY INFUSION PUMP
Manufacturer: MELANIE HESS
Device Classification Name: Pump, Infusion
Regulation Number: FRN
Classification Product Code: 06/14/2005
Date Received: 11/17/2005
Decision Date: Substantially Equivalent (SESE)
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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