# Columbus Instruments Intl. Corp.

- Location (FDA's records): Columbus, OH
- FDA decisions: 5 (1977–1990): 5 510(k) clearances
- Product codes: DXG (2), GYD (1), BZL (1), FLL (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
- K895791: Oxymax (Mar 28, 1990)
- K861543: Cardiomax-II (Mar 10, 1987)
- K861100: Iso-Thermex (May 12, 1986)
- K782036: Tremor Monitor (Jan 23, 1979)
- K771718: Cardiotherm-500X (Sep 28, 1977)

Source page: https://510kreport.com/company/columbus-instruments-intl