510(k) K151139 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
EasyMap MAP Catheter
| Applicant | Medfact Engineering GmbH, Loerrach, Baden-Wurttemberg, DE |
| Decision | Substantially Equivalent, Oct 18, 2016 |
| Received | Apr 29, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151139
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.