# Promedica, Inc.

- Location (FDA's records): Oldsmar, FL
- FDA decisions: 2 (2004–2004): 2 510(k) clearances
- Product codes: KCT (2)
- 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
- K032445: The Ultra System (Mar 29, 2004)
- K032813: The Ultra System SP (Feb 13, 2004)

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