510(k) K152999 ยท DXX System, Catheter Control, Steerable
CorPath 200 System
| Applicant | Corindus, Inc., Waltham MA, US |
| Decision | Substantially Equivalent, Mar 18, 2016 |
| Received | Oct 13, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152999
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.