510(k) K932306 ยท FFX System, Gastrointestinal Motility (Electrical)
MICROINFUSOR
| Applicant | Sandhill Scientific, Inc., Littleton CO, US |
| Decision | Substantially Equivalent, Apr 1, 1994 |
| Received | May 11, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932306
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.