ARTICLE | Clinical News
UTASWako i30 regulatory update
March 7, 2011 8:00 AM UTC
FDA granted 510(k) clearance for Wako's uTASWako i30 automated instrument for use with its FDA-cleared alpha-fetoprotein L3 (AFP-L3) and des-gamma-carboxy prothrombin (DCP) in vitro diagnostics to ass...