510(k) K935843 ยท FMI Needle, Hypodermic, Single Lumen
BE-SAFE
| Applicant | Mathis-Koolpe, Inc., Elkins Park PA, US |
| Decision | Substantially Equivalent, Jun 3, 1994 |
| Received | Dec 8, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935843
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.