510(k) K193632 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
LassoStar Circular Mapping Catheter
| Applicant | Biosense Webster, Inc., Irvin CA, US |
| Decision | Substantially Equivalent, Jun 30, 2020 |
| Received | Dec 27, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K193632
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.