510(k) K180797 ยท DQY Catheter, Percutaneous
Xcess Guiding Catheter
| Applicant | Curatia Medical Co., Santa Clara CA, US |
| Decision | Substantially Equivalent, Dec 14, 2018 |
| Received | Mar 27, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180797
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.