510(k) K210328 ยท DRC Trocar
SafeSept Blunt Needle
| Applicant | Pressure Products Medical Device Manufacturing, LLC, Morton PA, US |
| Decision | Substantially Equivalent, Mar 5, 2021 |
| Received | Feb 4, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K210328
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.