510(k) K191087 ยท FFX System, Gastrointestinal Motility (Electrical)
IntraMarX Radiopaque Markers
| Applicant | Anx Robotica Corp, Plano TX, US |
| Decision | Substantially Equivalent, Dec 18, 2019 |
| Received | Apr 24, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191087
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.