510(k) K162359 ยท DQY Catheter, Percutaneous
Surefire Guiding Catheter
| Applicant | Surefire Medical, Inc., Westminster CO, US |
| Decision | Substantially Equivalent, Sep 21, 2016 |
| Received | Aug 23, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K162359
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.