FDA 510(k) Application Details - K051285

Device Classification Name	Glucose Oxidase, Glucose   More FDA Info for this Device
510(K) Number	K051285
Device Name	Glucose Oxidase, Glucose
Applicant	INFOPIA CO., LTD 889-3, KWANYANG2-DONG, DONGAN-GU ANYANG KVUNGGI 431-716 KR Other 510(k) Applications for this Company
Contact	BYEONG WOO BAE 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	05/17/2005
Decision Date	08/02/2005
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