FDA 510(k) Application Details - K120921

Device Classification Name	Glucose Oxidase, Glucose   More FDA Info for this Device
510(K) Number	K120921
Device Name	Glucose Oxidase, Glucose
Applicant	SIMPLE DIAGNOSTICS, INC. 8870 RAVELLO CT NAPLES, FL 34114 US Other 510(k) Applications for this Company
Contact	DANIEL KAMM Other 510(k) Applications for this Contact
Regulation Number	862.1345   More FDA Info for this Regulation Number
Classification Product Code	CGA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/27/2012
Decision Date	08/21/2012
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