510(k) K160725 ยท FFX System, Gastrointestinal Motility (Electrical)
EndoFLIP
| Applicant | Crospon, Ltd., Galway, IE |
| Decision | Substantially Equivalent, May 1, 2016 |
| Received | Mar 16, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160725
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.