510(k) K122506 ยท DQX Wire, Guide, Catheter
SUREFIRE HIGH FLOW ANGIOGRAPHIC CATHETER, ACCESS
| Applicant | Surefire Medical, Inc., Miami FL, US |
| Decision | Substantially Equivalent, Sep 17, 2012 |
| Received | Aug 17, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122506
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.