NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach System) with NaviCam Stomach Capsule/Tether (NaviCam Xpress Stomach System with NaviCam Capsule/Tether)— 510(k) K241934
Substantially EquivalentAnx Robotica Corp
FDA 510(k) clearance K241934 for NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach System) with NaviCam Stomach Capsule/Tether (NaviCam Xpress Stomach System with NaviCam Capsule/Tether), Substantially Equivalent on 2024-07-31. Applicant: Anx Robotica Corp. Device class: 2.
Clearance details
- Applicant
- Anx Robotica Corp
- Product code
- Code QKZ
- Device class
- Class 2
- Regulation
- 21 CFR 876.1310
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Plano, TX, US
Recent devices under product code QKZ
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More clearances from Anx Robotica Corp
view allData sourced from openFDA. This site is unofficial and independent of the FDA.