510(k) K240007 ยท FFX System, Gastrointestinal Motility (Electrical)
Solar Compact (G4-1)
| Applicant | Laborie Medical Technologies, Corp., Portsmouth NH, US |
| Decision | Substantially Equivalent, May 6, 2024 |
| Received | Jan 2, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240007
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.