510(k) K002427 ยท FFX System, Gastrointestinal Motility (Electrical)
SANDHILL UNITIP CATHETER PRESSURE SENSOR, MODEL K 5251-L3-0026
| Applicant | Sandhill Scientific, Inc., Highlands Ranch CO, US |
| Decision | Substantially Equivalent, Jun 22, 2001 |
| Received | Aug 8, 2000 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K002427
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.