510(k) K040961 ยท FDI Snare, Flexible
INJECTOR NEEDLE/SNARE
| Applicant | United States Endoscopy Group, Inc., Mentor OH, US |
| Decision | Substantially Equivalent, Jul 8, 2004 |
| Received | Apr 13, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K040961
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.