510(k) K020891 ยท FDI Snare, Flexible
NAKAO SNARE II AND NAKAO SNARE III
| Applicant | Granit Medical Innovations, New York NY, US |
| Decision | Substantially Equivalent, Jun 17, 2002 |
| Received | Mar 19, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020891
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.