510(k) K242076 · DXF Catheter, Septostomy
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| Applicant | Baylis Medical Company, Mississauga, CA |
| Decision | Substantially Equivalent, Nov 1, 2024 |
| Received | Jul 16, 2024 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K242076
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.