# Dako Diagnostics, Ltd.

- Location (FDA's records): Cambridgeshire, GB
- FDA decisions: 6 (1993–1998): 6 510(k) clearances
- Product codes: GNW (2), GQP (1), LIQ (1), GQS (1), LJC (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: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K981226: Imagearainfluenza Virus Group (Types 1,2 and 3) Test and Imagen Parainfluenza Virus Test Types 1,2 and 3 (Sep 28, 1998)
- K973954: Imagen Respiratory Screen (Dec 22, 1997)
- K962037: Imagen Respiratory Screen (Dec 26, 1996)
- K940564: Ideia (TM) Chlamydia Blocking Reagents, Modification (Jan 11, 1996)
- K943557: Imagen (Jan 9, 1995)
- K932384: Ideia (TM) Rotavirus (Dec 27, 1993)

Source page: https://510kreport.com/company/dako-diagnostics