510(k) K221608 ยท QKZ Magnetically Maneuvered Capsule Endoscopy System
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
| Applicant | Anx Robotica Corp, Plano TX, US |
| Decision | Substantially Equivalent, Nov 22, 2022 |
| Received | Jun 3, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221608
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.