Device Classification Name |
System, Measurement, Blood-Pressure, Non-Invasive
More FDA Info for this Device |
510(K) Number |
K222125 |
Device Name |
System, Measurement, Blood-Pressure, Non-Invasive |
Applicant |
Shenzhen AOJ Medical Technology Co., Ltd.
Room 301&4F, Blk A, Building A, Jingfa IM Park
Xiaweiyuan, Gushu Community, Xixiang, Baoan
Shenzhen 518126 CN
Other 510(k) Applications for this Company
|
Contact |
Jack Wang
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 |
07/18/2022 |
Decision Date |
12/01/2022 |
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 |
|