510(k) K231010 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Corvair
| Applicant | AliveCor, Inc., Mountain View CA, US |
| Decision | Substantially Equivalent, Jun 7, 2024 |
| Received | Apr 7, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231010
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.