510(k) K231629 ยท DQY Catheter, Percutaneous
091 Balloon Guide Catheter
| Applicant | Eosolutions, Corp., Pembroke Pines FL, US |
| Decision | Substantially Equivalent, Oct 31, 2023 |
| Received | Jun 5, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K231629
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.