510(k) K241221 ยท NRY Catheter, Thrombus Retriever
CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter; Cerenovus Aspiration Tubing Set
| Applicant | Cerenovus, Inc., Miami FL, US |
| Decision | Substantially Equivalent, Oct 16, 2024 |
| Received | May 1, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241221
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.