510(k) K262398 ยท NRY Catheter, Thrombus Retriever
CEREGLIDE 57 Intermediate Catheter; Cerenovus Aspiration Tubing set
| Applicant | CERENOVUS, Inc., Miami FL, US |
| Decision | Substantially Equivalent, Aug 13, 2026 |
| Received | Jul 14, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K262398
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.