510(k) K943578 ยท FMI Needle, Hypodermic, Single Lumen
MONOJECT HIGH VOLUME/CHEMOTHERAPY SHARPS CONTAINER
| Applicant | Sherwood Medical Co., St. Louis MO, US |
| Decision | Substantially Equivalent, Aug 23, 1994 |
| Received | Jul 22, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K943578
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.