510(k) K112497 ยท DTK Filter, Intravascular, Cardiovascular
MERIDIAN FILTER SYSTEM - FEMORAL DELIVERY KIT
| Applicant | C.R. Bard, Inc., Tempe AZ, US |
| Decision | Substantially Equivalent, Oct 24, 2011 |
| Received | Aug 29, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K112497
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.