# Mitsubishi Kagaku Iatron

- Location (FDA's records): Seattle, WA
- FDA decisions: 4 (2008–2009): 4 510(k) clearances
- Product codes: NBC (1), GHH (1), DCN (1), JHX (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Mitsubishi Chemical Medience Corporation: 1 (https://510kreport.com/company/mitsubishi-chemical-medience)

## Its most-cited devices
- K081360: Pathfast CK-MB-II, Pathfast Myo-II (2009), cited by 1

## Recent decisions
- K081360: Pathfast CK-MB-II, Pathfast Myo-II (Aug 17, 2009)
- K072288: Pathfast D-Dimer (May 6, 2009)
- K083412: Pathfast Hscrp (Mar 9, 2009)
- K072189: Pathfast Ntprobnp and D-Dimer Tests (Feb 5, 2008)

Source page: https://510kreport.com/company/mitsubishi-kagaku-iatron