510(k) K230156 ยท DQY Catheter, Percutaneous
5F Launcher Guide Catheter, 6F Launcher Guide Catheter, 7F Launcher Guide Catheter, 8F Launcher Guide Catheter
| Applicant | Medtronic Vascular, Danvers MA, US |
| Decision | Substantially Equivalent, Jun 30, 2023 |
| Received | Jan 19, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K230156
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.