510(k) K172893 ยท DRC Trocar
SafeSept Needle Free Transseptal Guidewire
| Applicant | Pressure Products Medical Device Manufacturing, LLC, Morton PA, US |
| Decision | Substantially Equivalent, Dec 21, 2017 |
| Received | Sep 22, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172893
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.