510(k) K993995 ยท FMF Syringe, Piston
VEIN ENTRY INDICATOR DEVICE (VEID)
| Applicant | Vascular Technologies , Ltd., Ginot Shomron 44853, IL |
| Decision | Substantially Equivalent, Feb 14, 2000 |
| Received | Nov 24, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K993995
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.