Device Classification Name |
System, Imaging, Pulsed Doppler, Ultrasonic
More FDA Info for this Device |
510(K) Number |
K211886 |
Device Name |
System, Imaging, Pulsed Doppler, Ultrasonic |
Applicant |
Shenzhen Wisonic Medical Technology Co.Ltd.
1st, 2nd, 5th & 6th Floor, NO.6 Building,
Pingshan Technology Park, Taoyuan Street, Nanshan District
Shenzhen 518055 CN
Other 510(k) Applications for this Company
|
Contact |
Jiang Xiaosan
Other 510(k) Applications for this Contact |
Regulation Number |
892.1550
More FDA Info for this Regulation Number |
Classification Product Code |
IYN
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
Date Received |
06/21/2021 |
Decision Date |
12/02/2021 |
Decision |
SESE - SUBST EQUIV |
Classification Advisory Committee |
RA - Radiology |
Review Advisory Committee |
RA - Radiology |
Statement / Summary / Purged Status |
Summary |
Type |
Traditional |
Reviewed By Third Party |
N |
Expedited Review |
|