510(k) K960020 ยท FHN Ligator, Hemorrhoidal
SOLO BAND LIGATOR
| Applicant | Surcraft, LLC, Newport News VA, US |
| Decision | Substantially Equivalent, Apr 1, 1996 |
| Received | Jan 2, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960020
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.