FDA 510(k) Application Details - K023834

Device Classification Name	System, Measurement, Blood-Pressure, Non-Invasive   More FDA Info for this Device
510(K) Number	K023834
Device Name	System, Measurement, Blood-Pressure, Non-Invasive
Applicant	HEALTH & LIFE CO., LTD. 6F,NO.407, CHUNG SHAN RD. SEC.02, CHUNG HO CITY TAIPEI HSIEN 235 TW Other 510(k) Applications for this Company
Contact	SUSAN CHEN 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	11/18/2002
Decision Date	01/14/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	Y
Expedited Review