510(k) K182909 ยท FDI Snare, Flexible
Roth Net Retriever Product Line
| Applicant | United States Endoscopy Group, Inc., Mentor OH, US |
| Decision | Substantially Equivalent, Nov 21, 2018 |
| Received | Oct 17, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K182909
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.