510(k) K180517 ยท DXX System, Catheter Control, Steerable
CorPath GRX System
| Applicant | Corindus, Inc., Waltham MA, US |
| Decision | Substantially Equivalent, Mar 29, 2018 |
| Received | Feb 27, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K180517
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.