510(k) K201076 ยท QJP Catheter, Percutaneous, Neurovasculature
Anchor Dual Lumen Guidewire Catheter
| Applicant | Aqure Medical, Inc., Rogers MN, US |
| Decision | Substantially Equivalent, Aug 6, 2020 |
| Received | Apr 22, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201076
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.