K240578
- 510(k) number
- K240578
- Device name
- VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System
- Applicant
- B.Braun Medical, Inc. PA · US
- Product code
- DTK — Filter, Intravascular, Cardiovascular
- Decision date
- 2024-07-31
- Date received
- 2024-03-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
510(k) Summary (official FDA PDF): K240578.pdf
Official FDA record: K240578
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.