510(k) K062222 ยท FFX System, Gastrointestinal Motility (Electrical)
UNITIP HIGH RESOLUTION CATHETER
| Applicant | Unisensor AG, Golden CO, US |
| Decision | Substantially Equivalent, Mar 15, 2007 |
| Received | Aug 2, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062222
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.