510(k) K000433 ยท LKF Cannula, Manipulator/Injector, Uterine
PBN HYSTERO-SALPINGOGRAPHY CATHETER SET
| Applicant | Medical Device Technologies, Inc., Gainesville FL, US |
| Decision | Substantially Equivalent, Jun 16, 2000 |
| Received | Feb 9, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000433
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.