510(k) K901203 ยท FMF Syringe, Piston
HYPODERMIC SYRINGE LUER LOK
| Applicant | Ware-Medics Glass Works, Inc., Pearl River NY, US |
| Decision | Substantially Equivalent, Jun 6, 1990 |
| Received | Mar 14, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901203
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.