510(k) K972279 ยท FMI Needle, Hypodermic, Single Lumen
SHARPS SHUTTLE
| Applicant | Sage Products, Inc., Crystal Lake IL, US |
| Decision | Substantially Equivalent, Aug 29, 1997 |
| Received | Jun 18, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972279
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.