K231960 is an FDA 510(k) clearance for the NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach System) with NaviCam Capsule and NaviCam Tether, a Magnetically Maneuvered Capsule Endoscopy System (Class II — Special Controls, product code QKZ), submitted by Anx Robotica Corporation (Plano, US). The FDA issued a Cleared decision on October 3, 2023, 92 days after receiving the submission on July 3, 2023. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.1310.
| 510(k) Number | K231960 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | July 03, 2023 |
| Decision Date | October 03, 2023 |
| Days to Decision | 92 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | QKZ — Magnetically Maneuvered Capsule Endoscopy System |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 876.1310 |
| Definition | A Magnetically Maneuvered Capsule Endoscopy System Consists Of An Ingestible Capsule And Magnetic Controller And Is Used For Visualization Of The Stomach And Duodenum. The Ingestible Capsule Contains A Camera That Wirelessly Captures Images Of The Mucosa. The Magnetic Controller Is Used Outside Of The Patient And Is Magnetically Coupled With The Capsule To Control Its Location And Viewing Direction. |