FDA 510(k) Application Details - K161220

Device Classification Name	Respiratory Virus Panel Nucleic Acid Assay System   More FDA Info for this Device
510(K) Number	K161220
Device Name	Respiratory Virus Panel Nucleic Acid Assay System
Applicant	LUMINEX CORPORATION 12212 TECHNOLOGY BLVD AUSTIN, TX 78727 US Other 510(k) Applications for this Company
Contact	WENDY RICKER Other 510(k) Applications for this Contact
Regulation Number	866.3980   More FDA Info for this Regulation Number
Classification Product Code	OCC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/29/2016
Decision Date	08/02/2016
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	MI - Microbiology
Review Advisory Committee	MI - Microbiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review