510(k) K232354 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
Vios Monitoring System(TM) Model 2050; Vios Central Station Monitor/Vios Central Server Software
| Applicant | Murata Vios, Inc., Woodbury MN, US |
| Decision | Substantially Equivalent, Mar 22, 2024 |
| Received | Aug 7, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232354
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.