510(k) K120834 ยท DXX System, Catheter Control, Steerable
CORPATH 200 SYSTEM
| Applicant | Corindus, Inc., Baltimore MD, US |
| Decision | Substantially Equivalent, Jul 19, 2012 |
| Received | Mar 19, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120834
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.