# Cardionostics, Inc.

- Location (FDA's records): Tustin, CA
- FDA decisions: 4 (1984–1990): 4 510(k) clearances
- Product codes: DSH (4)
- 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
- K902486: Cardiovista (Aug 23, 1990)
- K863863: Cardionostics Holter Dura-Lite Recorder (Cassette) (Oct 15, 1986)
- K844977: Holter Cura-Lite Recorder (Jan 14, 1985)
- K842954: Cardionostics Holter Dura-Lite Recorde (Sep 4, 1984)

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