# Pronosco A/S

- Location (FDA's records): Washington, DC
- FDA decisions: 2 (2000–2000): 2 510(k) clearances
- Product codes: KGI (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (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 that cite its devices most
- Sectra-Imtec AB: 1 (https://510kreport.com/company/sectra-imtec)

## Its most-cited devices
- K002500: X-Posure System Version 2 Rad (2000), cited by 1

## Recent decisions
- K003656: X-Posure System Version 2 Mammo (Dec 15, 2000)
- K002500: X-Posure System Version 2 Rad (Oct 23, 2000)

Source page: https://510kreport.com/company/pronosco-a-s