# Cathaid, Inc.

- Location (FDA's records): Miami, FL
- FDA decisions: 3 (1986–1986): 3 510(k) clearances
- Product codes: KOD (1), KGZ (1), FGE (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
- K864115: Tubegripper, Drainage Catheter & Accessory for SU (Nov 7, 1986)
- K863958: Tubegripper, Urological Catheter & Accessory (Nov 4, 1986)
- K863957: Tubegripper, Drainage Catheter & Accessory for GU (Oct 24, 1986)

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