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. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K240578.
When did VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System receive FDA 510(k) clearance?
VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System received FDA 510(k) clearance on 2024-07-31, under 510(k) number K240578.
Who is the listed applicant for VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System?
The FDA 510(k) record lists B.Braun Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
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
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing B.Braun Medical, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: DTK)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.