510(k) K202275 ยท DXX System, Catheter Control, Steerable
CorPath GRX System
| Applicant | Corindus, Inc., Waltham MA, US |
| Decision | Substantially Equivalent, Dec 11, 2020 |
| Received | Aug 11, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202275
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.