VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System
K-Number: K240578 · 2024-07-31
Device Summary
Frequently Asked Questions
What is the VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System?
VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System is a medical device that received FDA 510(k) clearance on 2024-07-31. It is manufactured by B.Braun Medical, Inc.. The 510(k) number is K240578.
When was VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System approved by the FDA?
VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System received FDA 510(k) clearance on 2024-07-31, under approval number K240578.
What company makes VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System?
VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System is manufactured by B.Braun Medical, Inc..
What is the FDA product code for VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System?
The FDA product code for VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System is DTK.
Related Clinical Trials
Other Devices by B.Braun Medical, Inc.
Related Devices (Code: DTK)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.