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FDA 510(k), K010485, VENA TECH VENA CAVA FILTER; VENA TECH 30D VENA CAVA FILTER; VENA TECH LP CAVE FILTER
FDA 510(k), K010485, VENA TECH VENA CAVA FILTER; VENA TECH 30D VENA CAVA FILTER; VENA TECH LP CAVE FILTER
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510(K) Number: K010485
Device Name: VENA TECH VENA CAVA FILTER; VENA TECH 30D VENA CAVA FILTER; VENA TECH LP CAVE FILTER
Manufacturer: B BRAUN
Device Classification Name: Filter, Intravascular, Cardiovascular
Regulation Number: 870.3375
Classification Product Code: DTK
Date Received: 02/20/2001
Decision Date: 05/18/2001
Regulation Medical Specialty: Cardiovascular
Device Name: VENA TECH VENA CAVA FILTER; VENA TECH 30D VENA CAVA FILTER; VENA TECH LP CAVE FILTER
Manufacturer: B BRAUN
Device Classification Name: Filter, Intravascular, Cardiovascular
Regulation Number: 870.3375
Classification Product Code: DTK
Date Received: 02/20/2001
Decision Date: 05/18/2001
Regulation Medical Specialty: Cardiovascular
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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