510(k) K003580 ยท FFX System, Gastrointestinal Motility (Electrical)
UNITIP GASTROINTESTINAL PRESSURE SENSOR CATHETER
| Applicant | Unisensor AG, Golden CO, US |
| Decision | Substantially Equivalent, Jul 31, 2001 |
| Received | Nov 20, 2000 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K003580
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.