# Mogul Enterprises

- Location (FDA's records): San Jose, CA
- FDA decisions: 3 (2000–2003): 3 510(k) clearances
- Product codes: DRF (3)
- 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
- K030852: 4 French & 5 French Electrophysiology Diagnostic Catheters Models 5UEXXX, 5BEXXX and 5FEXXX, and 4UEXXX, 4BEXXX and 4FEX (Jul 10, 2003)
- K011734: 6-French, 20-Electrode Electrophysiology Diagnostic Catheter, Models 6U20XXX, 6B20XXX, and 6F20XXX (Jul 3, 2001)
- K993698: Slimcath-DX Models, 3SUXXXX, 3SBXXXX, and Fcxxxx (Aug 16, 2000)

Source page: https://510kreport.com/company/mogul-enterprises