510(k) K233982 ยท QJP Catheter, Percutaneous, Neurovasculature
CEREGLIDE 92 Catheter System
| Applicant | Cerenovus, Inc., Miami FL, US |
| Decision | Substantially Equivalent, May 9, 2024 |
| Received | Dec 18, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K233982
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.