FDA 510(k), K982182, FEMOSTOP II PLUS DISPOSABLE SET MODEL 11166, FEMOSTOP II PLUS COMPRESSION ARCH MODEL 11168, FEMOSTOP II BILATERAL ADAPT0
FDA 510(k), K982182, FEMOSTOP II PLUS DISPOSABLE SET MODEL 11166, FEMOSTOP II PLUS COMPRESSION ARCH MODEL 11168, FEMOSTOP II BILATERAL ADAPT0
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510(K) Number: K982182
Device Name: FEMOSTOP II PLUS DISPOSABLE SET MODEL 11166, FEMOSTOP II PLUS COMPRESSION ARCH MODEL 11168, FEMOSTOP II BILATERAL ADAPT0
Manufacturer: RADI MEDICAL SYSTEMS AB
Device Classification Name: clamp, vascular
Regulation Number: 870.4450
Classification Product Code: DXC
Date Received: 06/22/1998
Decision Date: 09/18/1998
Regulation Medical Specialty: Cardiovascular
Device Name: FEMOSTOP II PLUS DISPOSABLE SET MODEL 11166, FEMOSTOP II PLUS COMPRESSION ARCH MODEL 11168, FEMOSTOP II BILATERAL ADAPT0
Manufacturer: RADI MEDICAL SYSTEMS AB
Device Classification Name: clamp, vascular
Regulation Number: 870.4450
Classification Product Code: DXC
Date Received: 06/22/1998
Decision Date: 09/18/1998
Regulation Medical Specialty: Cardiovascular
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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