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FDA 510(k), K093659, ECLIPSE FILTER SYSTEM-FEMORAL DELIVERY KIT, ECLIPSE FILTER SYSTEM-JUGULAR/SUBCLAVIAN DELIVERY KIT MODEL RF500F MODEL RF5
FDA 510(k), K093659, ECLIPSE FILTER SYSTEM-FEMORAL DELIVERY KIT, ECLIPSE FILTER SYSTEM-JUGULAR/SUBCLAVIAN DELIVERY KIT MODEL RF500F MODEL RF5
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510(K) Number: K093659
Device Name: ECLIPSE FILTER SYSTEM-FEMORAL DELIVERY KIT, ECLIPSE FILTER SYSTEM-JUGULAR/SUBCLAVIAN DELIVERY KIT MODEL RF500F MODEL RF5
Manufacturer: C.R. BARD, INC.
Device Classification Name: filter, intravascular, cardiovascular
Regulation Number: 870.3375
Classification Product Code: DTK
Date Received: 11/25/2009
Decision Date: 01/14/2010
Regulation Medical Specialty: Cardiovascular
Device Name: ECLIPSE FILTER SYSTEM-FEMORAL DELIVERY KIT, ECLIPSE FILTER SYSTEM-JUGULAR/SUBCLAVIAN DELIVERY KIT MODEL RF500F MODEL RF5
Manufacturer: C.R. BARD, INC.
Device Classification Name: filter, intravascular, cardiovascular
Regulation Number: 870.3375
Classification Product Code: DTK
Date Received: 11/25/2009
Decision Date: 01/14/2010
Regulation Medical Specialty: Cardiovascular
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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