FDA 510(k) Application Details - K220220

Device Classification Name	System, Measurement, Blood-Pressure, Non-Invasive   More FDA Info for this Device
510(K) Number	K220220
Device Name	System, Measurement, Blood-Pressure, Non-Invasive
Applicant	Zhuhai Linte Medical Instrument Co., Ltd. 4th Floor, Building 1, No.66, Yongda Road, Hongqi Town, Jinwan District Zhuhai 519090 CN Other 510(k) Applications for this Company
Contact	Wallace Huang 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	01/26/2022
Decision Date	10/03/2022
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