510(k) K102214 ยท FFX System, Gastrointestinal Motility (Electrical)
ENDO FLIP
| Applicant | Crospon, Ltd., Bonita Springs FL, US |
| Decision | Substantially Equivalent, Dec 16, 2010 |
| Received | Aug 6, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102214
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.