FDA 510(k) Application Details - K051703

Device Classification Name	System, Measurement, Blood-Pressure, Non-Invasive   More FDA Info for this Device
510(K) Number	K051703
Device Name	System, Measurement, Blood-Pressure, Non-Invasive
Applicant	TaiDoc Technology Corporation 4F, 88, SEC.1, KWANG FU ROAD SAN CHUNG, TAIPEI 241 TW Other 510(k) Applications for this Company
Contact	SHU-MEI WU Other 510(k) Applications for this Contact
Regulation Number	870.1130   More FDA Info for this Regulation Number
Classification Product Code	DXN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/24/2005
Decision Date	08/12/2005
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review