# Cytocare, Inc.

- Location (FDA's records): Aliso Viejo, CA
- FDA decisions: 7 (1992–1995): 7 510(k) clearances
- Product codes: GEI (3), GEX (3), GEH (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Endocare, Inc.: 4 (https://510kreport.com/company/endocare)

## Its most-cited devices
- K942299: Endocare Cryotherapy System (1995), cited by 2
- K952587: Endocare Monopolar Electrodes (1995), cited by 1
- K954321: Endocare Monopolar Electrodes (Modification) (1995), cited by 1

## Recent decisions
- K954321: Endocare Monopolar Electrodes (Modification) (Oct 13, 1995)
- K952698: Endocare Electrosurgical Handpiece (Aug 14, 1995)
- K952587: Endocare Monopolar Electrodes (Jul 17, 1995)
- K942299: Endocare Cryotherapy System (Jan 19, 1995)
- K945054: Endocare Prolase I Advanced Laser Delivery System (Nov 28, 1994)
- K934211: Cytocare Diode Laser System (May 17, 1994)
- K921708: Cytocare Laser Catheter for Urology (Oct 1, 1992)

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