510(k) K981733 ยท FFX System, Gastrointestinal Motility (Electrical)
DIGITRAPPER DELTA, MODEL 9043G0201 AND POLYGRAM '98 PH EXTENSION MODEL 9043S0111
| Applicant | Medtronic Functional Diagnostics A/S, Skovlunde, DK |
| Decision | Substantially Equivalent, Feb 4, 1999 |
| Received | May 18, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981733
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 20, 2004 | Medtronic Gastroenterology / Urology Medtronic Gastro pH in a Box System, Model 43A008, Catalog Number 9043A0081 Terminated |
FFX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.