510(k) K153481 ยท NGT Saline, Vascular Access Flush
0.9% Sodium Chloride Injection, USP BD PosiFlush SF Syringe
| Applicant | Becton, Dickinson and Company, Franklin Lakes NJ, US |
| Decision | Substantially Equivalent, Apr 4, 2016 |
| Received | Dec 3, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K153481
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Apr 16, 2020 | Becton Dickinson & Company BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553), UDI 50382903065535 Terminated |
NGT | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.