510(k) K974363 ยท FMI Needle, Hypodermic, Single Lumen
BECTON DICKINSON BLUNT PLASTIC CANNULA
| Applicant | Bd Becton Dickinson Vacutainer Systems Preanalytic, Franklin Lakes NJ, US |
| Decision | Substantially Equivalent, Jun 3, 1998 |
| Received | Nov 19, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K974363
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 5, 2015 | Becton Dickinson & Company BD 10 mL Syringe BD Luer-Lok Tip with Blunt Plastic Cannula, Not for Skin Injection ; Catalog #303348,
BD 10 mL Syringe Luer-Lok Tip with Blunt Fill Needle 18G x 1 1/2 (1.2mm x 40 mm), not for skin Terminated |
FMF | None listed |
| Sep 9, 2006 | Becton Dickinson & Company BD Vacutainer Blood Collection Assembly with BD Blunt Plastic Cannula; Catalog #303380. Terminated |
FMI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.