510(k) K093866 ยท DRA Catheter, Steerable
EVALVE STEERABLE GUIDE CATHETER
| Applicant | Evalve, Inc., Menlo Park CA, US |
| Decision | Substantially Equivalent, Jan 13, 2010 |
| Received | Dec 17, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K093866
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.