510(k) K001115 ยท LKF Cannula, Manipulator/Injector, Uterine
ULTRA CATHETER SET
| Applicant | Lyco Enterprises, Inc., El Paso TX, US |
| Decision | Substantially Equivalent, May 17, 2000 |
| Received | Apr 6, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001115
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.