# Kabi Diagnostica

- Location (FDA's records): Danville, CA
- FDA decisions: 2 (1990–1990): 2 510(k) clearances
- Product codes: JBQ (1), KFF (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
- K902393: Coacute Antithrombin Chromogenic Assay (Sep 25, 1990)
- K901874: Coatest LMW Heparin/Heparin Chromogenic Assay (Jul 20, 1990)

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