FDA 510(k) Application Details - K062800

Device Classification Name	System, Test, Blood Glucose, Over The Counter   More FDA Info for this Device
510(K) Number	K062800
Device Name	System, Test, Blood Glucose, Over The Counter
Applicant	TaiDoc Technology Corporation 4F, 88, SEC.1, KWANG FU ROAD SAN CHUNG, TAIPEI 241 TW Other 510(k) Applications for this Company
Contact	PI-SHIOU LI 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	09/19/2006
Decision Date	01/12/2007
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