510(k) K142598 ยท DQX Wire, Guide, Catheter
Opto Wire and OptoMonitor System
| Applicant | Opsens, Inc., Quebec, CA |
| Decision | Substantially Equivalent, Jun 12, 2015 |
| Received | Sep 15, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142598
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.