510(k) K212473 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
Welch Allyn Connex Central Station
| Applicant | Welch Allyn, Inc., Skaneateles Falls NY, US |
| Decision | Substantially Equivalent, Oct 28, 2022 |
| Received | Aug 6, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212473
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.