MotiliCap GI Monitoring System— 510(k) K250493
Substantially EquivalentAnx Robotica Corporation
FDA 510(k) clearance K250493 for MotiliCap GI Monitoring System, Substantially Equivalent on 2025-05-21. Applicant: Anx Robotica Corporation.
Clearance details
- Applicant
- Anx Robotica Corporation
- Product code
- Code NYV
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Plano, TX, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.