FDA 510(k) Application Details - K160990

Device Classification Name	More FDA Info for this Device
510(K) Number	K160990
Device Name	Nova Max Uric Acid Monitoring System
Applicant	NOVA BIOMEDICAL CORPORATION 200 PROSPECT STREET WALTHAM, MA 02454 US Other 510(k) Applications for this Company
Contact	ELIZA WANG Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	PTC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/08/2016
Decision Date	04/11/2017
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review