510(k) K191907 ยท DQX Wire, Guide, Catheter
OptoWire III
| Applicant | Opsens, Inc., Quebec, CA |
| Decision | Substantially Equivalent, Jan 2, 2020 |
| Received | Jul 16, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191907
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.