FDA 510(k) Application Details - K141755

Device Classification Name	System, Measurement, Blood-Pressure, Non-Invasive   More FDA Info for this Device
510(K) Number	K141755
Device Name	System, Measurement, Blood-Pressure, Non-Invasive
Applicant	SEJOY ELECTRONICS & INSTRUMENTS CO., LTD. BLDG 2, NO. 202, ZHENZHONG RD WEST LAKE ECONOMY & TECH ZONE HANGZHOU, ZHEJIANG 310030 CN Other 510(k) Applications for this Company
Contact	REN YUNHUA 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	06/30/2014
Decision Date	11/19/2014
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review