510(k) K895890 ยท FMF Syringe, Piston
AUTOPEN
| Applicant | Ulster Scientific, Inc., Highland NY, US |
| Decision | Substantially Equivalent, Feb 16, 1990 |
| Received | Oct 5, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895890
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.