510(k) K973911 ยท FMI Needle, Hypodermic, Single Lumen
2 GALLON ALTERNATE CARE SHARPS CONTAINER
| Applicant | Sage Products, Inc., Crystal Lake IL, US |
| Decision | Substantially Equivalent, Oct 29, 1997 |
| Received | Oct 14, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973911
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.