510(k) K123258 ยท LKF Cannula, Manipulator/Injector, Uterine
THE ADVANCE CATHETER FOR HSG AND SIS
| Applicant | Catheter Research, Inc., Indianapolis IN, US |
| Decision | Substantially Equivalent, Jan 31, 2013 |
| Received | Oct 18, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K123258
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.