510(k) K130104 ยท DQX Wire, Guide, Catheter
GUIDEWIRE, PURSUER SERIES
| Applicant | Oscor, Inc., Palm Harbor FL, US |
| Decision | Substantially Equivalent, Jun 13, 2013 |
| Received | Jan 15, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130104
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.