510(k) K230214 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
Huma RPM (RPM)
| Applicant | Medopad, Inc., New York NY, US |
| Decision | Substantially Equivalent, Jun 2, 2023 |
| Received | Jan 26, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230214
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.