510(k) K880581 ยท FFX System, Gastrointestinal Motility (Electrical)
AMBUL. PH & MOTILITY RECORDER FOR MEASURE OF PARA.
| Applicant | Synectics-Dantec, Irving TX, US |
| Decision | Substantially Equivalent, Aug 11, 1988 |
| Received | Feb 10, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880581
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.