510(k) K192037 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
Advisor VL Circular Mapping Catheter, Sensor Enabled
| Applicant | ABBOTT MEDICAL, Plymouth MN, US |
| Decision | Substantially Equivalent, Sep 17, 2019 |
| Received | Jul 30, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K192037
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.