510(k) K190980 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
Reprocessed Webster Duo-Decapolar Diagnostic EP Catheter
| Applicant | Innovative Health, LLC, Scottsdale AZ, US |
| Decision | Substantially Equivalent, Jul 1, 2019 |
| Received | Apr 15, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190980
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.