510(k) K991288 ยท FFX System, Gastrointestinal Motility (Electrical)
DISTENDER SERIES II BAROSTAT
| Applicant | G & J Electronics, Inc., Toronto, Ontario, CA |
| Decision | Substantially Equivalent, Jun 8, 1999 |
| Received | Apr 14, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991288
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.