510(k) K931122 ยท LKF Cannula, Manipulator/Injector, Uterine
OVAMED HSG CATHETER
| Applicant | Ovamed Corp., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Jan 30, 1995 |
| Received | Mar 4, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931122
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.