# Technia Diagnostics, Ltd.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 9 (1979–1986): 9 510(k) clearances
- Product codes: KTL (1), CDD (1), JMF (1), CGR (1), KHQ (1), CDX (1), LCS (1), CDP (1), LCQ (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
- K861978: Autofluor V (Jun 10, 1986)
- K801843: T3(125) Radioimmunoassay Kit (Sep 16, 1980)
- K801202: Digoxin Radioimmunoassay Kit (Jun 20, 1980)
- K801203: Cortisol Radioimmunoassay Kit (Jun 9, 1980)
- K791361: T3 Uptake Radioimmunoassay Kit (Aug 16, 1979)
- K790919: HPL Ria Kit (Jun 28, 1979)
- K790495: Thyroxine Ria Kit (May 3, 1979)
- K782024: Ria Kit, Vitamin B12 (Feb 28, 1979)

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