510(k) K140917 ยท DYB Introducer, Catheter
INTRODUCER, MODEL ADELANTE MAGNUM
| Applicant | Oscor, Inc., Palm Harbor FL, US |
| Decision | Substantially Equivalent, Jul 9, 2014 |
| Received | Apr 10, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K140917
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.