510(k) K221707 · DRC Trocar
SafeSept® Transseptal Guidewire (SS-140)
| Applicant | Pressure Products Medical Device Manufacturing, LLC, Morton PA, US |
| Decision | Substantially Equivalent, Sep 14, 2022 |
| Received | Jun 13, 2022 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K221707
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.