AMDI Submits Groundbreaking Dual 510(k) and CLIA Waiver Application to FDA Autonomous Medical Devices Incorporated (AMDI) has submitted a dual 510(k) and CLIA Waiver application for its Fast PCR mini respiratory panel aimed at rapid diagnostics.

AMDI Submits Groundbreaking Dual 510(k) and CLIA Waiver Application to FDA #FDA_Submission #AMDI #Fast_PCR_Mini

AliveDx Takes Significant Steps with FDA Submission for MosaiQ AiPlex® Vasculitis Assay AliveDx has officially submitted its MosaiQ AiPlex® Vasculitis assay for FDA clearance, aspiring to enhance diagnostic solutions for autoimmune vasculitis, improving patient outcomes.

AliveDx Takes Significant Steps with FDA Submission for MosaiQ AiPlex® Vasculitis Assay #USA #AliveDx #Eysins #MosaiQ_AiPlex #FDA_Submission