510(k) K170833 · FFX System, Gastrointestinal Motility (Electrical)
EndoFLIP® System with FLIP Topography module
| Applicant | Crospon, Ltd., Galway, IE |
| Decision | Substantially Equivalent, Apr 17, 2017 |
| Received | Mar 20, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K170833
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.