510(k) K241244 ยท QJP Catheter, Percutaneous, Neurovasculature
CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter
| Applicant | Cerenovus, Inc., Miami FL, US |
| Decision | Substantially Equivalent, Oct 16, 2024 |
| Received | May 2, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241244
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.