510(k) K190833 ยท DQY Catheter, Percutaneous
AXS Vecta Aspiration Catheter
| Applicant | Stryker Neurovascular, Fremont CA, US |
| Decision | Substantially Equivalent, Dec 15, 2019 |
| Received | Apr 1, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190833
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.