Last synced on 30 May 2025 at 11:05 pm

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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241934
510(k) Type
Special
Applicant
AnX Robotica Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2024
Days to Decision
29 days
Submission Type
Summary

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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241934
510(k) Type
Special
Applicant
AnX Robotica Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2024
Days to Decision
29 days
Submission Type
Summary