FDA 510(k), K141654, THE BELMONT RAPID INFUSER
FDA 510(k), K141654, THE BELMONT RAPID INFUSER
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510(K) Number: K141654
Device Name: THE BELMONT RAPID INFUSER
Manufacturer: BELMONT INSTRUMENT CORPORATION
Device Classification Name: Pump, Infusion
Regulation Number: 880.5725
Classification Product Code: FRN
Date Received: 06/20/2014
Decision Date: 07/18/2014
Regulation Medical Specialty: General Hospital
Device Name: THE BELMONT RAPID INFUSER
Manufacturer: BELMONT INSTRUMENT CORPORATION
Device Classification Name: Pump, Infusion
Regulation Number: 880.5725
Classification Product Code: FRN
Date Received: 06/20/2014
Decision Date: 07/18/2014
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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