510(k) K231861 ยท FFX System, Gastrointestinal Motility (Electrical)
EndoflipTM 300 System
| Applicant | Covidien, LLC, Santa Clara CA, US |
| Decision | Substantially Equivalent, Jul 21, 2023 |
| Received | Jun 23, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K231861
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.