510(k) K242392 ยท QJP Catheter, Percutaneous, Neurovasculature
PATH BGC
| Applicant | Crossroads Neurovascular, Inc., Lake Forest CA, US |
| Decision | Substantially Equivalent, May 9, 2025 |
| Received | Aug 12, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242392
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.