510(k) K160866 ยท DTK Filter, Intravascular, Cardiovascular
Denali Filter System - Femoral Delivery Kit, Denali Filter System - Jugular/Subclavian Delivery Kit
| Applicant | C.R. Bard, Inc., Tempe AZ, US |
| Decision | Substantially Equivalent, Apr 29, 2016 |
| Received | Mar 30, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K160866
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.