FDA 510(k) Application Details - K191180

Device Classification Name	System, Measurement, Blood-Pressure, Non-Invasive   More FDA Info for this Device
510(K) Number	K191180
Device Name	System, Measurement, Blood-Pressure, Non-Invasive
Applicant	Shenzhen AOJ Medical Technology Co., Ltd. 601, 6th floor, B2 Building, An'le Industrial Park #172 Hangcheng Avenue Shenzhen 518126 CN Other 510(k) Applications for this Company
Contact	Qihuan Zhao 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	05/02/2019
Decision Date	08/23/2019
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