FDA 510(k) Application Details - K183491

Device Classification Name	System, Measurement, Blood-Pressure, Non-Invasive   More FDA Info for this Device
510(K) Number	K183491
Device Name	System, Measurement, Blood-Pressure, Non-Invasive
Applicant	Xuzhou Yongkang Electronic Science Technology Co., Ltd 4F Building C8, 40 Jingshan Road, Economic and Technological Development Zo Xuzhou 221009 CN Other 510(k) Applications for this Company
Contact	Kai Li 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	12/17/2018
Decision Date	03/24/2019
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