510(k) K201750 ยท MTD Catheter, Intracardiac Mapping, High-Density Array
Pentaray Nav eco High-Density Mapping Catheter
| Applicant | Biosense Webster, Inc., Irvin CA, US |
| Decision | Substantially Equivalent, Aug 6, 2020 |
| Received | Jun 26, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201750
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.