510(k) K182075 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
BeneVision N Series Patient Monitors (Including BeneVision N12, BeneVision N15, BeneVision N17, BeneVision N19. BeneVision N22, BeneVision N1)
| Applicant | Shenzhen Mindray Bio-Medical Electronics Co., Ltd., Shenzhen, TW |
| Decision | Substantially Equivalent, Dec 10, 2018 |
| Received | Aug 1, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182075
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.