510(k) K113737 ยท DQO Catheter, Intravascular, Diagnostic
SUREFIRE GUIDE SHEATH
| Applicant | Surefire Medical, Inc., Miami FL, US |
| Decision | Substantially Equivalent, Feb 23, 2012 |
| Received | Dec 20, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K113737
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.