510(k) K905154 ยท FFX System, Gastrointestinal Motility (Electrical)
GASTROSCAN
| Applicant | Medics Instrument Corp., Solothurn, Switzerland, SE |
| Decision | Substantially Equivalent, Jun 19, 1991 |
| Received | Nov 15, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K905154
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.