Last synced on 25 January 2026 at 3:41 am

MotiliCap GI Monitoring System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250493
510(k) Type
Traditional
Applicant
Anx Robotica Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/2025
Days to Decision
90 days
Submission Type
Summary

MotiliCap GI Monitoring System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250493
510(k) Type
Traditional
Applicant
Anx Robotica Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/2025
Days to Decision
90 days
Submission Type
Summary