B.Braun Medical, Inc. · Class II · Cleared Jul 31, 2024
| K-number | K240578 |
| Device name | VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System |
| Applicant | B.Braun Medical, Inc. |
| Product code | DTK |
| Device class | Class II |
| Decision date | Jul 31, 2024 |
| Decision | Substantially Equivalent |
| Regulation | 870.3375 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov