# Cardiogenes

- Location (FDA's records): Palo Alto, CA
- FDA decisions: 20 (1992–1997): 20 510(k) clearances
- Product codes: GEX (20)
- 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
- K961560: Eclipse 2000 (Jan 27, 1997)
- K955006: Eclipse 2100 (Jan 17, 1996)
- K952755: Powersculptor Probes (Sep 14, 1995)
- K953658: Corssfire Plus (Aug 21, 1995)
- K953424: Eclipse 3200 (Aug 11, 1995)
- K945126: Eclipse 3200 (Jan 18, 1995)
- K944758: Sunrise Technologies Model 5020 PLDD Kit (Dec 27, 1994)
- K944153: Eclipse 3200 (Nov 9, 1994)

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