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FDA 510(k), K073090, RECOVERY G2 FILTER SYSTEM - FEMORAL DELIVERY KIT, MODEL RF-310F; JUGULAR/SUBCLAVAIN DELIVERY KIT, MODEL RF-320J
FDA 510(k), K073090, RECOVERY G2 FILTER SYSTEM - FEMORAL DELIVERY KIT, MODEL RF-310F; JUGULAR/SUBCLAVAIN DELIVERY KIT, MODEL RF-320J
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510(K) Number: K073090
Device Name: RECOVERY G2 FILTER SYSTEM - FEMORAL DELIVERY KIT, MODEL RF-310F; JUGULAR/SUBCLAVAIN DELIVERY KIT, MODEL RF-320J
Manufacturer: C.R. BARD, INC.
Device Classification Name: filter, intravascular, cardiovascular
Regulation Number: 870.3375
Classification Product Code: DTK
Date Received: 11/01/2007
Decision Date: 01/15/2008
Regulation Medical Specialty: Cardiovascular
Device Name: RECOVERY G2 FILTER SYSTEM - FEMORAL DELIVERY KIT, MODEL RF-310F; JUGULAR/SUBCLAVAIN DELIVERY KIT, MODEL RF-320J
Manufacturer: C.R. BARD, INC.
Device Classification Name: filter, intravascular, cardiovascular
Regulation Number: 870.3375
Classification Product Code: DTK
Date Received: 11/01/2007
Decision Date: 01/15/2008
Regulation Medical Specialty: Cardiovascular
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