510(k) K151623 ยท NRY Catheter, Thrombus Retriever
Penumbra System 110 Aspiration Tubing
| Applicant | Penumbra, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, Aug 6, 2015 |
| Received | Jun 16, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K151623
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.