510(k) K262392 ยท DQY Catheter, Percutaneous
APRO 35 Swift Catheter
| Applicant | Alembic, LLC, Mountain View CA, US |
| Decision | Substantially Equivalent, Aug 12, 2026 |
| Received | Jul 14, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K262392
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.