510(k) K122416 ยท FMF Syringe, Piston
ARTIGLASS L. O.R. GLASS SYRINGE
| Applicant | Artiglass Srl, Due Carrare Padova, IT |
| Decision | Substantially Equivalent, May 3, 2013 |
| Received | Aug 8, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122416
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.