510(k) K242104 ยท NRY Catheter, Thrombus Retriever
Penumbra System (Reperfusion Catheter RED 72)
| Applicant | Penumbra, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, Feb 13, 2025 |
| Received | Jul 18, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242104
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.