510(k) K251325 · DRE Dilator, Vessel, For Percutaneous Catheterization
VersaCross Connect Transseptal Dilator
| Applicant | Baylis Medical Company, Inc., Mississauga, CA |
| Decision | Substantially Equivalent, May 29, 2025 |
| Received | Apr 29, 2025 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K251325
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.