# Eurodiagnostica

- Location (FDA's records): Frederick, MD
- FDA decisions: 3 (2005–2005): 3 510(k) clearances
- Product codes: MOB (2), NHX (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (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
- Euro-Diagnostica AB: 2 (https://510kreport.com/company/euro-diagnostica)
- Roche Diagnostics Corp.: 1 (https://510kreport.com/company/roche-diagnostics)
- Orgentec Diagnostika GmbH: 1 (https://510kreport.com/company/orgentec-diagnostika)

## Its most-cited devices
- K052133: Immunoscan RA Anti-CCP Test System (2005), cited by 4

## Recent decisions
- K052133: Immunoscan RA Anti-CCP Test System (Dec 12, 2005)
- K051455: Wieslab Cap Mpo-Anca (Nov 23, 2005)
- K051458: Wieslab Cap PR-3 Anca (Nov 22, 2005)

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