510(k) K943485 ยท FMI Needle, Hypodermic, Single Lumen
MONOJECT HORIZONTAL ENTRY SHARPS CONTAINER
| Applicant | Sherwood Medical Co., St. Louis MO, US |
| Decision | Substantially Equivalent, Sep 9, 1994 |
| Received | Jul 19, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K943485
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.