510(k) K182522 ยท NRY Catheter, Thrombus Retriever
Penumbra System (Modified 110 Aspiration Tubing)
| Applicant | Penumbra, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, Oct 12, 2018 |
| Received | Sep 13, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K182522
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.