510(k) K220632 ยท DQY Catheter, Percutaneous
Boss Crossing Support Catheter
| Applicant | Marvao Medical Devices, Ltd., Galway, IE |
| Decision | Substantially Equivalent, Jun 2, 2022 |
| Received | Mar 4, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220632
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.