510(k) K183649 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
Diagnostic Fixed Electrophysiology Catheter, Diagnostic Electrophysiology Cable
| Applicant | Baylis Medical Company, Inc., Mississauga, CA |
| Decision | Substantially Equivalent, Jun 7, 2019 |
| Received | Dec 26, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183649
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.