510(k) K071405 ยท LKF Cannula, Manipulator/Injector, Uterine
PROBE HOLDER SYSTEM
| Applicant | Intuitive Surgical, Inc., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Oct 9, 2007 |
| Received | May 21, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071405
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.