510(k) K062563 ยท HDC Tenaculum, Uterine
FEMTEN CERVICAL TENACULUM
| Applicant | Fem Suite, LLC, Port Townsend WA, US |
| Decision | Substantially Equivalent, May 18, 2007 |
| Received | Aug 31, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062563
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.