FDA 510(k) Application Details - K102751

Device Classification Name	System, Test, Blood Glucose, Over The Counter   More FDA Info for this Device
510(K) Number	K102751
Device Name	System, Test, Blood Glucose, Over The Counter
Applicant	CERAGEM MEDISYS INC. 3699 WILSHIRE BLVD., STE 930 LOS ANGELES, CA 90010 US Other 510(k) Applications for this Company
Contact	GRACE KIM 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	09/23/2010
Decision Date	02/11/2013
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