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FDA 510(k), K925679, VENA CAVA FILTER SYSTEMS, MODIFICATION
FDA 510(k), K925679, VENA CAVA FILTER SYSTEMS, MODIFICATION
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510(K) Number: K925679
Device Name: VENA CAVA FILTER SYSTEMS, MODIFICATION
Manufacturer: PAUL O'CONNELL
Device Classification Name: Filter, Intravascular, Cardiovascular
Regulation Number: DTK
Classification Product Code: 11/10/1992
Date Received: 11/27/1992
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
Device Name: VENA CAVA FILTER SYSTEMS, MODIFICATION
Manufacturer: PAUL O'CONNELL
Device Classification Name: Filter, Intravascular, Cardiovascular
Regulation Number: DTK
Classification Product Code: 11/10/1992
Date Received: 11/27/1992
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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