510(k) K010485 ยท DTK Filter, Intravascular, Cardiovascular
VENA TECH VENA CAVA FILTER; VENA TECH 30D VENA CAVA FILTER; VENA TECH LP CAVE FILTER
| Applicant | Bbraun, Evanston IL, US |
| Decision | Substantially Equivalent, May 18, 2001 |
| Received | Feb 20, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010485
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 24, 2007 | B. Braun Interventional Systems Vena Tech LP Vena Cava Filter System, Item No/REF. 05010024, Model No: 40DLP, B Braun. Manufacturer: B. Braun Medical 204, avenue du Marechal Juin BP 331 92107 Boulogne Cedex , France. (The VenaTech L Terminated |
DTK | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.