FDA 510(k) Application Details - K231303

Device Classification Name	System, Measurement, Blood-Pressure, Non-Invasive   More FDA Info for this Device
510(K) Number	K231303
Device Name	System, Measurement, Blood-Pressure, Non-Invasive
Applicant	Joytech Healthcare Co., Ltd No.365, Wuzhou Road, Yuhang Economic Development Zone Hangzhou 311100 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	05/05/2023
Decision Date	01/26/2024
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