510(k) K961878 ยท FMI Needle, Hypodermic, Single Lumen
SHARPS-TAINER
| Applicant | Winfield Industries, Brentwood TN, US |
| Decision | Substantially Equivalent, Jun 27, 1996 |
| Received | May 15, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961878
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.