# Cogent Diagnotics, Ltd.

- Location (FDA's records): Midlothian, Scotland, GB
- FDA decisions: 31 (1992–2000): 31 510(k) clearances
- Product codes: LLL (7), MID (3), DHR (3), JNL (3), MST (2), JZO (2), MOB (2), LRM (1), MVJ (1), DDC (1), LKO (1), LKP (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K003054: Autostat II Ena-6 Profile Elisa (Oct 13, 2000)
- K003057: Autostat II Ena-4 Profile Elisa (Oct 13, 2000)
- K002215: Autostat II Anti-Myeloperoxidase (Mpo) Elisa (Sep 28, 2000)
- K993557: Autostat II Rheumatoid Factor Iga Elisa (Mar 3, 2000)
- K994338: Autostat II Rheumatoid Factor Igm Elisa (Feb 3, 2000)
- K993085: Autostat II Anti-Cardiolipin Screen Elisa (Feb 1, 2000)
- K993304: Autostat II Rheumatoid Factor Igg Elisa (Dec 6, 1999)
- K992449: Autostat II Anti-Cardiolipin Igm Elisa (Nov 24, 1999)

Source page: https://510kreport.com/company/cogent-diagnotics