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FDA 510(k), K063217, VENATECH LP BRACHIAL INTRODUCER SYSTEM (ANTECUBITAL)
FDA 510(k), K063217, VENATECH LP BRACHIAL INTRODUCER SYSTEM (ANTECUBITAL)
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510(K) Number: K063217
Device Name: VENATECH LP BRACHIAL INTRODUCER SYSTEM (ANTECUBITAL)
Manufacturer: B. BRAUN MEDICAL, INC.
Device Classification Name: Filter, Intravascular, Cardiovascular
Regulation Number: 870.3375
Classification Product Code: DTK
Date Received: 10/24/2006
Decision Date: 01/12/2007
Regulation Medical Specialty: Cardiovascular
Device Name: VENATECH LP BRACHIAL INTRODUCER SYSTEM (ANTECUBITAL)
Manufacturer: B. BRAUN MEDICAL, INC.
Device Classification Name: Filter, Intravascular, Cardiovascular
Regulation Number: 870.3375
Classification Product Code: DTK
Date Received: 10/24/2006
Decision Date: 01/12/2007
Regulation Medical Specialty: Cardiovascular
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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