510(k) K943740 ยท FMI Needle, Hypodermic, Single Lumen
ROLL-A-WAY SHARPS DISPOSAL SYSTEM (RED AND IVORY)
| Applicant | Premium Plastics, Inc., Chicago IL, US |
| Decision | Substantially Equivalent, Dec 14, 1994 |
| Received | Aug 2, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K943740
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.