510(k) K123439 ยท OCY Endoscopic Guidewire, Gastroenterology-Urology
NEO ERCP GUIDEWIRE
| Applicant | Neometrics, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Jan 3, 2013 |
| Received | Nov 8, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123439
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.