510(k) K083594 ยท LKF Cannula, Manipulator/Injector, Uterine
EZ HSG CATHETER.FOAMSEAL CATHETER
| Applicant | Obg Products, Vienna VA, US |
| Decision | Substantially Equivalent, Jul 21, 2009 |
| Received | Dec 5, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083594
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.