510(k) K182829 ยท DQY Catheter, Percutaneous
Scepter Mini Occlusion Balloon Catheter
| Applicant | MicroVention, Inc., Aliso Viejo CA, US |
| Decision | Substantially Equivalent, Jul 10, 2019 |
| Received | Oct 5, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182829
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.