510(k) K232111 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
NeoBeat, NeoBeat Mini
| Applicant | Laerdal Medical AS, Stavanger, NO |
| Decision | Substantially Equivalent, Jun 25, 2024 |
| Received | Jul 14, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232111
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.