510(k) K935434 ยท LKF Cannula, Manipulator/Injector, Uterine
OBSTETRIC-GYNECOLOGIC SPECIALIZED MANUAL INSTRUMENT
| Applicant | United States Surgical, A Division of Tyco Healthc, Norwalk CT, US |
| Decision | Substantially Equivalent, May 27, 1994 |
| Received | Nov 10, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935434
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.