510(k) K980179 ยท FMI Needle, Hypodermic, Single Lumen
SHARPS PLUS 5 GALLON SHARPS CONTAINER
| Applicant | Rotonics Mfg., Inc., Bensenville IL, US |
| Decision | Substantially Equivalent, Apr 13, 1998 |
| Received | Jan 20, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980179
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.