510(k) K250962 ยท DQY Catheter, Percutaneous
APRO 55 Intermediate Catheter
| Applicant | Alembic, LLC, Mountain View CA, US |
| Decision | Substantially Equivalent, Apr 29, 2025 |
| Received | Mar 31, 2025 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K250962
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.