510(k) K133513 ยท FDI Snare, Flexible
MULTI-STAGE SNARE
| Applicant | United States Endoscopy Group, Inc., Mentor OH, US |
| Decision | Substantially Equivalent, Dec 20, 2013 |
| Received | Nov 12, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K133513
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.