510(k) K251877 ยท FIE Needle, Fistula
JMS CAVEO A.V. Fistula Needle Set
| Applicant | JMS North America Corporation, Hayward CA, US |
| Decision | Substantially Equivalent, Aug 15, 2025 |
| Received | Jun 18, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K251877
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.