510(k) K121677 ยท DQO Catheter, Intravascular, Diagnostic
SUREFIRE HI-FLOW MICROCATHETER
| Applicant | Surefire Medical, Inc., Miami FL, US |
| Decision | Substantially Equivalent, Jun 14, 2012 |
| Received | Jun 7, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121677
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.