510(k) K022503 ยท LKF Cannula, Manipulator/Injector, Uterine
UTERINE INJECTOR
| Applicant | Thomas Medical, Inc., Alpharetta GA, US |
| Decision | Substantially Equivalent, Oct 25, 2002 |
| Received | Jul 29, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022503
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.