510(k) K240320 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Patient Monitor (RespArray)
| Applicant | Edan Instruments, Inc., Shenzhen, CN |
| Decision | Substantially Equivalent, Jun 28, 2024 |
| Received | Feb 2, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240320
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.