510(k) K170032 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
QMAPP Amplifier; QMAPP Hemodynamic Monitoring System; QMAPP PCM; QMAPP GO; QMAPP EP
| Applicant | Fysicon BV, Oss, NL |
| Decision | Substantially Equivalent, Sep 8, 2017 |
| Received | Jan 4, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170032
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.