510(k) K221113 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
Accutorr 3 Vital Signs Monitor, Rosebud Vital Signs Monitor
| Applicant | Shenzhen Mindray Bio-Medical Electronics Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Dec 2, 2022 |
| Received | Apr 15, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221113
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.