# Irex Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 10 (1977–1985): 10 510(k) clearances
- Product codes: IYO (2), DXK (1), DSF (1), IYN (1), CDP (1), JAF (1), DPW (1), DQK (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
- K844404: Irex PS, Portable Scanner and 118 (Feb 4, 1985)
- K843643: Color Doppler 880 (Jan 31, 1985)
- K842408: Irex 730 Mechanical Sector Scanner (Nov 29, 1984)
- K840139: Irex 720 Sector Scanner (May 9, 1984)
- K827370: Irex System II 2D/Doppler Imaging System (Jun 28, 1982)
- K813544: Irex 2D/Doppler Phase Array Imaging Sys. (Feb 5, 1982)
- K811246: Doppler Ultrasound Blood Flowmeter (Aug 12, 1981)
- K792525: Irex Cardioplan (Dec 27, 1979)

Source page: https://510kreport.com/company/irex