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NaviCam Capsule Endoscope System with NaviCam Stomach Capsule and NaviCam Tether, NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach System) with NaviCam Stomach 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
K221608
510(k) Type
Traditional
Applicant
AnX Robotica Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/2022
Days to Decision
172 days
Submission Type
Summary

NaviCam Capsule Endoscope System with NaviCam Stomach Capsule and NaviCam Tether, NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach System) with NaviCam Stomach 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
K221608
510(k) Type
Traditional
Applicant
AnX Robotica Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/2022
Days to Decision
172 days
Submission Type
Summary