510(k) K152840 ยท DQY Catheter, Percutaneous
Lantern Delivery Microcatheter
| Applicant | Penumbra, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, Dec 2, 2015 |
| Received | Sep 29, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K152840
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.