510(k) K210009 ยท DQY Catheter, Percutaneous
Guiding Catheter
| Applicant | CenterPoint Systems, LLC, West Valley City UT, US |
| Decision | Substantially Equivalent, Nov 24, 2021 |
| Received | Jan 4, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210009
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.