# Vitalcare, Inc.

- Location (FDA's records): Miami, FL
- FDA decisions: 3 (2003–2003): 3 510(k) clearances
- Product codes: GBM (1), EZD (1), EZL (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
- K021938: Vitalcare Urethral Catheter (Apr 22, 2003)
- K021939: Vitalcare Foley Catheter (Apr 22, 2003)
- K023872: Vitalcare Urethral Catheter Red Rubber (Apr 10, 2003)

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