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. Device class: 2.
Clearance details
- Applicant
- Anx Robotica Corporation
- Product code
- Code NYV
- Device class
- Class 2
- Regulation
- 21 CFR 876.1725
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Plano, TX, US
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