# Clinical Data Instruments, Inc.

- Location (FDA's records): Walker, MI
- FDA decisions: 3 (1983–1985): 3 510(k) clearances
- Product codes: DSH (1), IOQ (1), DRJ (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
- K842349: Ambulatory PH Recording Device (Jun 14, 1985)
- K832828: Centurion Cardiac Detector (May 9, 1984)
- K832829: Neo-Float Neonatal Flotation Sys & Rhyt (Oct 4, 1983)

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