510(k) K100081 ยท FED Endoscopic Access Overtube, Gastroenterology-Urology
ENTEROSCOPY OVERTUBE, MODEL 00712140
| Applicant | United States Endoscopy Group, Inc., Mentor OH, US |
| Decision | Substantially Equivalent, Apr 12, 2010 |
| Received | Jan 12, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100081
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.