510(k) K082305 ยท DTK Filter, Intravascular, Cardiovascular
G2 EXPRESS FILTER SYSTEM - FEMORAL AND JUGULAR/SUBCLAVIAN DELIVERY KITS
| Applicant | C.R. Bard, Inc., Tempe AZ, US |
| Decision | Substantially Equivalent, Oct 31, 2008 |
| Received | Aug 13, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K082305
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.