510(k) K933981 ยท LKF Cannula, Manipulator/Injector, Uterine
CERVICAL CATHETER
| Applicant | Conceptus, Inc., San Carlos CA, US |
| Decision | Substantially Equivalent, Dec 27, 1994 |
| Received | Aug 16, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933981
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.