510(k) K233988 ยท NRY Catheter, Thrombus Retriever
Cerenovus Large Bore Catheter; Cerenovus Aspiration Tubing Set
| Applicant | Cerenovus, Inc., Miami FL, US |
| Decision | Substantially Equivalent, Jan 17, 2024 |
| Received | Dec 18, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K233988
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.