# Regulatory Consultants TO the Medical Device Indus

- Location (FDA's records): Sandy, UT
- FDA decisions: 1 (1994–1994): 1 510(k) clearance
- Product codes: KPX (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
- K935157: Articulated, Laparoscopic, and Side-Viewing T-Probes (Aug 9, 1994)

Source page: https://510kreport.com/company/regulatory-consultants-to-the-medical-device-indus