510(k) K854877 ยท FMF Syringe, Piston
ACU-SYRINGE W/WO NEEDLES
| Applicant | Acuderm, Inc., Ft Lauderdale FL, US |
| Decision | Substantially Equivalent, Feb 19, 1986 |
| Received | Dec 6, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854877
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.