510(k) K202405 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
BeneVision N12, BeneVision N15, BeneVision N17, BeneVision N19, BeneVision N22, BeneVision N1
| Applicant | Shenzhen Mindray Bio-Medical Electronics Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Jan 7, 2021 |
| Received | Aug 21, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202405
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.