# Celltech Diagnostics, Ltd.

- Location (FDA's records): Suite 11oo, Washington, DC
- FDA decisions: 1 (1991–1991): 1 510(k) clearance
- Product codes: MHI (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
- K912152: Cellabs Giardia Cel I.F. Test (Aug 12, 1991)

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