510(k) K760761 ยท FFX System, Gastrointestinal Motility (Electrical)
ESOPHAGEAL MOTILITY TUBE
| Applicant | Sherwood Medical Industries, Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 30, 1976 |
| Received | Oct 4, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K760761
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.