510(k) K222000 ยท FFX System, Gastrointestinal Motility (Electrical)
Transit-Pellets
| Applicant | Medifactia AB, Stockholm, SE |
| Decision | Substantially Equivalent, Jan 18, 2023 |
| Received | Jul 7, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222000
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.