Last synced on 30 May 2025 at 11:05 pm

NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach System) with NaviCam Capsule and NaviCam Tether

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231960
510(k) Type
Traditional
Applicant
AnX Robotica Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2023
Days to Decision
92 days
Submission Type
Summary

NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach System) with NaviCam Capsule and NaviCam Tether

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231960
510(k) Type
Traditional
Applicant
AnX Robotica Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2023
Days to Decision
92 days
Submission Type
Summary