FDA 510(k) Application Details - K173140

Device Classification Name	System, Test, Blood Glucose, Over The Counter   More FDA Info for this Device
510(K) Number	K173140
Device Name	System, Test, Blood Glucose, Over The Counter
Applicant	VivaChek Laboratories, Inc. 913 N Market Street, Suite 200 Wilmington, DE 19081 US Other 510(k) Applications for this Company
Contact	Julie Zhou Other 510(k) Applications for this Contact
Regulation Number	862.1345   More FDA Info for this Regulation Number
Classification Product Code	NBW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/29/2017
Decision Date	12/19/2018
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
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