# Qompium NV

- Location (FDA's records): Hasselt, BE
- FDA decisions: 2 (2018–2024): 2 510(k) clearances
- Product codes: QME (1), DXH (1)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 4 (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
- Advanced Fluidics, LLC: 1 (https://510kreport.com/company/advanced-fluidics)

## Firms that cite its devices most
- Measure Labs, Inc. (Dba Preemptiveai, Inc.): 1 (https://510kreport.com/company/measure-labs-dba-preemptiveai)
- Livmor: 1 (https://510kreport.com/company/livmor)
- Verily Life Sciences, LLC: 1 (https://510kreport.com/company/verily-life-sciences)

## Its most-cited devices
- K173872: FibriCheck (2018), cited by 3
- K232804: FibriCheck (2024), cited by 1

## Recent decisions
- K232804: FibriCheck (Jun 7, 2024)
- K173872: FibriCheck (Sep 28, 2018)

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