Class Class II

VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System (K240578)

K240578 2024-07-31 Traditional
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Description

VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System by B.Braun Medical, Inc. — FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK240578
Clearance Date2024-07-31
Clearance TypeTraditional
Product CodeDTK
Regulation Number870.3375

Categories

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