# Kmi Diagnostics, Inc.

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 6 (1997–2002): 6 510(k) clearances
- Product codes: JKR (1), CDZ (1), JLS (1), CHP (1), JKC (1), CGR (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
- K010790: Cortisol Lia (Jan 29, 2002)
- K990073: Calcitonin (May 11, 1999)
- K973900: Testoterone Elisa (Feb 24, 1998)
- K973901: 17 B-Estradiol (Elisa) (Nov 24, 1997)
- K973898: Progesterone Elisa (Nov 13, 1997)
- K973897: DHEA-S (Nov 13, 1997)

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