510(k) K973844 ยท FFX System, Gastrointestinal Motility (Electrical)
GASTRIC AND RECTAL CATHETERS
| Applicant | G & J Electronics, Inc., Toronto, Ontario, CA |
| Decision | Substantially Equivalent, Jun 4, 1999 |
| Received | Oct 8, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973844
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.