510(k) K944757 ยท FMI Needle, Hypodermic, Single Lumen
PISTON SYRINGES
| Applicant | Bd Becton Dickinson Vacutainer Systems Preanalytic, San Jose CA, US |
| Decision | Substantially Equivalent, Jan 11, 1995 |
| Received | Sep 27, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K944757
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 1, 2019 | Becton Dickinson & Company 3mL Safety-Lok Syringe, Catalog Number 309606, UDI 30382903096061 Terminated |
FMI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.