510(k) K232852 ยท DXF Catheter, Septostomy
Cross Vascular RF Transseptal Needle, Cross Vascular Connection Cable
| Applicant | Cross Vascular, Inc., Solana Beach CA, US |
| Decision | Substantially Equivalent, Oct 12, 2023 |
| Received | Sep 14, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232852
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.