510(k) K190574 ยท DSI Detector And Alarm, Arrhythmia
Patient Assistant Model PA97000
| Applicant | Medtronic, Inc., Mounds View MN, US |
| Decision | Substantially Equivalent, Sep 24, 2019 |
| Received | Mar 6, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190574
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.