510(k) K062887 ยท DTK Filter, Intravascular, Cardiovascular
MODIFICATION TO G2 FILTER SYSTEM-FEMORAL DELIVERY KIT, MODEL RF-310F
| Applicant | Bard Peripheral Vascular, Tempe AZ, US |
| Decision | Substantially Equivalent, Oct 26, 2006 |
| Received | Sep 26, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K062887
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.