# Fysicon BV

- Location (FDA's records): Oss, NL
- FDA decisions: 2 (2017–2025): 2 510(k) clearances
- Product codes: MWI (2)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Mckesson Israel, Ltd.: 2 (https://510kreport.com/company/mckesson-israel)
- Ge Medical Systems Information Technologies: 1 (https://510kreport.com/company/ge-medical-systems-information-technologies)

## Its most-cited devices
- K170032: QMAPP Amplifier; QMAPP Hemodynamic Monitoring System; QMAPP PCM; QMAPP GO; QMAPP EP (2017), cited by 1

## Recent decisions
- K241766: QMAPP®  (Hemo, Hemo Lite, PCM, GO, Hybrid) (Aug 27, 2025)
- K170032: QMAPP Amplifier; QMAPP Hemodynamic Monitoring System; QMAPP PCM; QMAPP GO; QMAPP EP (Sep 8, 2017)

Source page: https://510kreport.com/company/fysicon