510(k) K823701 ยท FFX System, Gastrointestinal Motility (Electrical)
MOTILITY CATHETERS
| Applicant | Mui Scientific, Mississauga, Ontario, CA |
| Decision | Substantially Equivalent, Feb 15, 1983 |
| Received | Dec 8, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823701
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.