510(k) K130906 ยท FFX System, Gastrointestinal Motility (Electrical)
ENDOFLIP CATHETER
| Applicant | Crospon, Ltd., Bonita Springs FL, US |
| Decision | Substantially Equivalent, Jul 17, 2013 |
| Received | Apr 1, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130906
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.