510(k) K240864 ยท DQX Wire, Guide, Catheter
PacePro Wire
| Applicant | Opsens, Inc., Quebec, CA |
| Decision | Substantially Equivalent, May 24, 2024 |
| Received | Mar 28, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240864
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.