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FDA 510(k), K983471, FEMOSTOP COMPRESSION ARCH, FEMOSTOP PUMP, FEMOSTOP BILATERAL ADAPTER
FDA 510(k), K983471, FEMOSTOP COMPRESSION ARCH, FEMOSTOP PUMP, FEMOSTOP BILATERAL ADAPTER
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510(K) Number: K983471
Device Name: FEMOSTOP COMPRESSION ARCH, FEMOSTOP PUMP, FEMOSTOP BILATERAL ADAPTER
Manufacturer: RADI MEDICAL SYSTEMS AB
Device Classification Name: clamp, vascular
Regulation Number: 870.4450
Classification Product Code: DXC
Date Received: 10/02/1998
Decision Date: 02/23/1999
Regulation Medical Specialty: Cardiovascular
Device Name: FEMOSTOP COMPRESSION ARCH, FEMOSTOP PUMP, FEMOSTOP BILATERAL ADAPTER
Manufacturer: RADI MEDICAL SYSTEMS AB
Device Classification Name: clamp, vascular
Regulation Number: 870.4450
Classification Product Code: DXC
Date Received: 10/02/1998
Decision Date: 02/23/1999
Regulation Medical Specialty: Cardiovascular
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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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