510(k) K023051 ยท LKF Cannula, Manipulator/Injector, Uterine
INTRAUTERINE DELIVERY SYSTEM - INJECTOR
| Applicant | Prosurg, Inc., San Jose CA, US |
| Decision | Substantially Equivalent, Dec 12, 2002 |
| Received | Sep 13, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023051
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.