510(k) K240177 · DSI Detector And Alarm, Arrhythmia
Zio AT® device (A100A1001)
| Applicant | iRhythm Technologies, Inc., San Francisco CA, US |
| Decision | Substantially Equivalent, Oct 30, 2024 |
| Received | Jan 23, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240177
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.