510(k) K902975 ยท LKF Cannula, Manipulator/Injector, Uterine
TWIN BALLOON INJECTOR
| Applicant | Zinnanti Surgical Instruments, Inc., Chatsworth CA, US |
| Decision | Substantially Equivalent, Sep 26, 1990 |
| Received | Jul 6, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902975
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.