510(k) K234115 ยท DQY Catheter, Percutaneous
APRO 55 Catheter
| Applicant | Alembic, LLC, Mountain View CA, US |
| Decision | Substantially Equivalent, Mar 15, 2024 |
| Received | Dec 27, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K234115
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.