510(k) K945809 ยท FMI Needle, Hypodermic, Single Lumen
MONOJECT(R) VERTICAL ENTRY SHARPS CONTAINER (1 QT)
| Applicant | Sherwood Medical Co., St. Joseph MO, US |
| Decision | Substantially Equivalent, Mar 15, 1995 |
| Received | Nov 28, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K945809
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.