510(k) K063611 ยท LKF Cannula, Manipulator/Injector, Uterine
SALINE/ CONTRAST MEDIA INFUSION CATHETER
| Applicant | Utah Medical Products, Inc., Midvale UT, US |
| Decision | Substantially Equivalent, May 23, 2007 |
| Received | Dec 3, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K063611
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.