510(k) K004040 ยท FFX System, Gastrointestinal Motility (Electrical)
REDTECH GIPC 2000
| Applicant | Red-Tech, Inc., Laguna Niguel CA, US |
| Decision | Substantially Equivalent, Mar 29, 2001 |
| Received | Dec 29, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K004040
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.