# Cardio Data

- Location (FDA's records): Mchenry, IL
- FDA decisions: 6 (1977–1985): 6 510(k) clearances
- Product codes: DSH (3), DSI (2), DXH (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
- K853262: Cardio Data Pacerecorder PR3 (Oct 11, 1985)
- K850136: Cardio Data MK4 Holter Analysis System (Feb 1, 1985)
- K834257: Cardiodata Pace Recorder (Jan 30, 1984)
- K831184: Cardio Data Pacemaker Recorder (May 9, 1983)
- K812149: Cardio-Data System, #Mark Iii (Aug 31, 1981)
- K770264: Paceguard (Feb 16, 1977)

Source page: https://510kreport.com/company/cardio-data