510(k) K170671 ยท DRC Trocar
SafeSept Transseptal Guidewire
| Applicant | Pressure Products Medical Device Manufacturing, LLC, Morton PA, US |
| Decision | Substantially Equivalent, Oct 20, 2017 |
| Received | Mar 6, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170671
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.