510(k) K233350 ยท DQY Catheter, Percutaneous
SINC Support Catheter
| Applicant | Reflow Medical, Inc., San Clemente CA, US |
| Decision | Substantially Equivalent, Feb 8, 2024 |
| Received | Sep 29, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233350
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.