# Diatech Diagnostica, Ltd.

- Location (FDA's records): Washington, DC
- FDA decisions: 3 (1988–1989): 3 510(k) clearances
- Product codes: LJZ (2), JXA (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
- K895276: Diatech Igm-MP Test (Dec 18, 1989)
- K882596: MP Test (Jun 21, 1989)
- K882211: Uriscreen (Sep 30, 1988)

Source page: https://510kreport.com/company/diatech-diagnostica