510(k) K083793 ยท DRA Catheter, Steerable
STEERABLE GUIDE CATHETER
| Applicant | Evalve, Inc., Menlo Park CA, US |
| Decision | Substantially Equivalent, Apr 27, 2009 |
| Received | Dec 22, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083793
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.