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FDA 510(k), K874096, TITANIUM GREENFIELD VENA CAVA FILTER CARRIER
FDA 510(k), K874096, TITANIUM GREENFIELD VENA CAVA FILTER CARRIER
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510(K) Number: K874096
Device Name: TITANIUM GREENFIELD VENA CAVA FILTER CARRIER
Manufacturer: MEDI-TECH, INC.
Device Classification Name: filter, intravascular, cardiovascular
Regulation Number: 870.3375
Classification Product Code: DTK
Date Received: 10/08/1987
Decision Date: 11/04/1988
Regulation Medical Specialty: Cardiovascular
Device Name: TITANIUM GREENFIELD VENA CAVA FILTER CARRIER
Manufacturer: MEDI-TECH, INC.
Device Classification Name: filter, intravascular, cardiovascular
Regulation Number: 870.3375
Classification Product Code: DTK
Date Received: 10/08/1987
Decision Date: 11/04/1988
Regulation Medical Specialty: Cardiovascular
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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