# Ganshorn Medizin Electronic GmbH

- Location (FDA's records): Niederlauer, DE
- FDA decisions: 2 (2016–2024): 2 510(k) clearances
- Product codes: JEH (1), BZG (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 0 (0 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
- Viasys Healthcare GmbH: 1 (https://510kreport.com/company/viasys-healthcare)
- Ndd Medical Technologies: 1 (https://510kreport.com/company/ndd-medical-technologies)

## Recent decisions
- K240706: PowerCube+ Series (PowerCube Body+); PowerCube+ Series (PowerCube Diffusion+); PowerCube+ Series (PowerCube Body+ / Diffusion+) (Dec 9, 2024)
- K160116: SpiroScout (Oct 7, 2016)

Source page: https://510kreport.com/company/ganshorn-medizin-electronic