510(k) K221351 ยท DQX Wire, Guide, Catheter
Mechanical Guidewire
| Applicant | Baylis Medical Company, Inc., Mississauga, CA |
| Decision | Substantially Equivalent, Dec 19, 2022 |
| Received | May 10, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221351
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.