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NaviCam Small Bowel Capsule Endoscopy System with NaviCam SB 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
K233229
510(k) Type
Traditional
Applicant
AnX Robotica Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/5/2024
Days to Decision
99 days
Submission Type
Summary

NaviCam Small Bowel Capsule Endoscopy System with NaviCam SB 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
K233229
510(k) Type
Traditional
Applicant
AnX Robotica Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/5/2024
Days to Decision
99 days
Submission Type
Summary