510(k) K211219 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
LASSOSTAR NAV Circular Mapping Catheter
| Applicant | Biosense Webster, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Jan 26, 2022 |
| Received | Apr 23, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211219
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.