510(k) K192625 ยท DQY Catheter, Percutaneous
PG Pro Microcatheter
| Applicant | MicroVention, Inc. A TERUMO Group Company, Aliso Viejo CA, US |
| Decision | Substantially Equivalent, Nov 21, 2019 |
| Received | Sep 23, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K192625
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.