# Circadian, Inc.

- Location (FDA's records): San Jose, CA
- FDA decisions: 13 (1980–1992): 13 510(k) clearances
- Product codes: DPS (4), DSI (3), DSH (2), KRC (2), IYP (1), BZG (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
- K921878: Scanmate Iii (Sep 11, 1992)
- K894956: Circamed Holter Version 4 (Feb 5, 1990)
- K874641: Circadian Stress Test II (Apr 1, 1988)
- K874155: Circamed Monitor Remote Start Conductance Meter (Nov 23, 1987)
- K871251: Circamed Full Disclosure System (May 22, 1987)
- K860973: Circadian Stress Test System (Aug 25, 1986)
- K851517: Circa Med Single-Channel-Ambulatory Cardiac Monito (Oct 2, 1985)
- K851643: Remote Control Module (Sep 9, 1985)

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