FDA 510(k) Application Details - K241578

Device Classification Name	System, Measurement, Blood-Pressure, Non-Invasive   More FDA Info for this Device
510(K) Number	K241578
Device Name	System, Measurement, Blood-Pressure, Non-Invasive
Applicant	Shenzhen BSX Technology Electronics Co., Ltd. Rm101&2/F~4/F, Building No.13, Ailian Industrial park, Wulian Community, Longgang Distric Shenzhen 518116 CN Other 510(k) Applications for this Company
Contact	XiYu Lu 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	06/03/2024
Decision Date	02/19/2025
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