510(k) K160121 ยท DXX System, Catheter Control, Steerable
CorPath GRX System
| Applicant | Corindus, Inc., Waltham MA, US |
| Decision | Substantially Equivalent, Oct 27, 2016 |
| Received | Jan 19, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160121
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.