Fysicon BV
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2025-08-27
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K241766 | QMAPP® (Hemo, Hemo Lite, PCM, GO, Hybrid) | MWI | 2025-08-27 | View |
| 510(k) | K170032 | QMAPP Amplifier; QMAPP Hemodynamic Monitoring System; QMAPP PCM; QMAPP GO; QMAPP EP | MWI | 2017-09-08 | View |
No matching devices.