FDA 510(k) Application Details - K223291

Device Classification Name	System, Measurement, Blood-Pressure, Non-Invasive   More FDA Info for this Device
510(K) Number	K223291
Device Name	System, Measurement, Blood-Pressure, Non-Invasive
Applicant	Shenzhen Pango Medical Electronics Co., Ltd. No. 25, 1st Industry Zone, Fenghuang Road, Xikeng Village Henggang Town, Longgang District Shenzhen 518115 CN Other 510(k) Applications for this Company
Contact	Xiaoyun Yang 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	10/26/2022
Decision Date	06/14/2023
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