510(k) K251802 ยท GXI Probe, Radiofrequency Lesion
STAR RF Ablation System
| Applicant | Merit Medical Systems, Inc., South Jordan UT, US |
| Decision | Substantially Equivalent, Feb 13, 2026 |
| Received | Jun 12, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K251802
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.