510(k) K093659 ยท DTK Filter, Intravascular, Cardiovascular
ECLIPSE FILTER SYSTEM-FEMORAL DELIVERY KIT, ECLIPSE FILTER SYSTEM-JUGULAR/SUBCLAVIAN DELIVERY KIT MODEL RF500F MODEL RF5
| Applicant | C.R. Bard, Inc., Tempe AZ, US |
| Decision | Substantially Equivalent, Jan 14, 2010 |
| Received | Nov 25, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K093659
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.