510(k) K202066 ยท DQK Computer, Diagnostic, Programmable
EnSite X EP System, Advisor VL Circular Mapping Catheter, Sensor Enabled, Advisor FL Circular Mapping Catheter, Sensor Enabled, Advisor HD Grid High Density Mapping Catheter, Senor Enabled
| Applicant | ABBOTT MEDICAL, St. Paul MN, US |
| Decision | Substantially Equivalent, Nov 25, 2020 |
| Received | Jul 27, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202066
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.