510(k) K083690 ยท LKF Cannula, Manipulator/Injector, Uterine
FEMVUE(TM) CATHETER SYSTEM
| Applicant | Femasys, Inc., Suwanee GA, US |
| Decision | Substantially Equivalent, Jun 23, 2009 |
| Received | Dec 12, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083690
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.