510(k) K982541 ยท FMI Needle, Hypodermic, Single Lumen
VACUTAINER BRAND ECLIPSE BLOOD COLLECTION NEEDLE, MODELS# 368607 & 368608
| Applicant | Becton Dickinson Vacutainer Systems, Franklin Lake NJ, US |
| Decision | Substantially Equivalent, Oct 28, 1998 |
| Received | Jul 21, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982541
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Oct 31, 2019 | Becton Dickinson & Company BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25, cat. no. 368608 Terminated |
FMI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.