510(k) K100662 ยท LKF Cannula, Manipulator/Injector, Uterine
FEMVUE CORNUAL BALLOON CATHETER
| Applicant | Femasys, Inc., Suwanee GA, US |
| Decision | Substantially Equivalent, Apr 7, 2010 |
| Received | Mar 8, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K100662
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.