510(k) K171355 ยท DQO Catheter, Intravascular, Diagnostic
Surefire Precision Infusion System
| Applicant | Surefire Medical, Inc., Westminster CO, US |
| Decision | Substantially Equivalent, May 17, 2017 |
| Received | May 9, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K171355
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.