QMAPP Amplifier; QMAPP Hemodynamic Monitoring System; QMAPP PCM; QMAPP GO; QMAPP EP
Fysicon BV
FYSICON BV
FDA Registration(s)
| Registration | FEI | Name | Status | Initial importer | Expiration year | Address |
|---|---|---|---|---|---|---|
| 3010716438 | 3010716438 | FYSICON BV | 1 | N | 2026-01-01 | Hoogheuvelstraat 114 Oss Noord-Brabant NL 5349BA |
Registered Device Listings
| Registration key | Listing key | Premarket submission | Device | Product code | Decision date |
|---|---|---|---|---|---|
| 173658 | 1895095009 | K241766 | QMAPP® (Hemo, Hemo Lite, PCM, GO, Hybrid) | MWI | 2025-08-27 |
| 173658 | 2063907652 | K170032 | QMAPP Amplifier; QMAPP Hemodynamic Monitoring System; QMAPP PCM; QMAPP GO; QMAPP EP | MWI | 2017-09-08 |
| 173658 | 1360265795 |
Product Codes Associated With Registrations
| Product code | Registration listing records | Latest decision |
|---|---|---|
| MWI | 2 | 2025-08-27 |