510(k) K214080 ยท NGT Saline, Vascular Access Flush
Pentaflush
| Applicant | Pentaferte Italia S.R.L., Campli Teramo, IT |
| Decision | Substantially Equivalent, Jul 20, 2022 |
| Received | Dec 27, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K214080
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.