510(k) K261938 ยท QJP Catheter, Percutaneous, Neurovasculature
APRO 88 Catheter
| Applicant | Alembic, LLC, Mountain View CA, US |
| Decision | Substantially Equivalent, Oct 6, 2026 |
| Received | Jun 10, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K261938
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.