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FDA 510(k), K032426, GUNHTER TULIP VENA CAVA MREYE FILTER AND RETRIEVAL SET
FDA 510(k), K032426, GUNHTER TULIP VENA CAVA MREYE FILTER AND RETRIEVAL SET
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510(K) Number: K032426
Device Name: GUNHTER TULIP VENA CAVA MREYE FILTER AND RETRIEVAL SET
Manufacturer: JENNIFER J BOSLEY
Device Classification Name: Filter, Intravascular, Cardiovascular
Regulation Number: DTK
Classification Product Code: 08/06/2003
Date Received: 10/31/2003
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
Device Name: GUNHTER TULIP VENA CAVA MREYE FILTER AND RETRIEVAL SET
Manufacturer: JENNIFER J BOSLEY
Device Classification Name: Filter, Intravascular, Cardiovascular
Regulation Number: DTK
Classification Product Code: 08/06/2003
Date Received: 10/31/2003
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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