510(k) K070881 ยท FHN Ligator, Hemorrhoidal
LEM HEMORRHOIDAL LIGATOR, MODELS A.5650, A.5660
| Applicant | Sapimed S.P.A., Crofton MD, US |
| Decision | Substantially Equivalent, Sep 26, 2007 |
| Received | Mar 30, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070881
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.