510(k) K232562 ยท PDU Catheter For Crossing Total Occlusions
PowerWire Radiofrequency Guidewire Kit
| Applicant | Baylis Medical Technologies, Inc., Mississauga, CA |
| Decision | Unknown, Feb 28, 2024 |
| Received | Aug 24, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232562
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.