510(k) K241766 · MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
QMAPP® (Hemo, Hemo Lite, PCM, GO, Hybrid)
| Applicant | Fysicon BV, Oss, NL |
| Decision | Substantially Equivalent, Aug 27, 2025 |
| Received | Jun 20, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241766
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.