510(k) K250972 ยท DQY Catheter, Percutaneous
Primum Hydrophilic Guiding Catheter
| Applicant | Pendracare, Leek, NL |
| Decision | Substantially Equivalent, Jun 29, 2025 |
| Received | Mar 31, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250972
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.