510(k) K895432 ยท FMI Needle, Hypodermic, Single Lumen
SAFE-T-CAP
| Applicant | Ausmedics Pty , Ltd., Washington DC, US |
| Decision | Substantially Equivalent, Nov 3, 1989 |
| Received | Sep 8, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895432
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.