FDA 510(k) Application Details - K062033

Device Classification Name	System, Measurement, Blood-Pressure, Non-Invasive   More FDA Info for this Device
510(K) Number	K062033
Device Name	System, Measurement, Blood-Pressure, Non-Invasive
Applicant	KING YIELD HONGKONG LIMITED 12 FL, NO. 180 ELECTRIC ROAD NORTH POINT HK Other 510(k) Applications for this Company
Contact	DACHENG GONG 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	07/18/2006
Decision Date	03/23/2007
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	Y
Expedited Review