510(k) K250493 ยท NYV Gastrointestinal Motility System, Capsule
MotiliCap GI Monitoring System
| Applicant | Anx Robotica Corporation, Plano TX, US |
| Decision | Substantially Equivalent, May 21, 2025 |
| Received | Feb 20, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250493
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.