510(k) K881609 ยท FFX System, Gastrointestinal Motility (Electrical)
SITZMARKS
| Applicant | Lafayette Pharmacal, Inc., Lafayette IN, US |
| Decision | Substantially Equivalent, Jul 8, 1988 |
| Received | Apr 12, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881609
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.