Device Classification Name |
System, Imaging, Pulsed Doppler, Ultrasonic
More FDA Info for this Device |
510(K) Number |
K172082 |
Device Name |
System, Imaging, Pulsed Doppler, Ultrasonic |
Applicant |
Sonoscape Medical Corp.
4/f, 5/f, 8/f, 9/f & 10/f
Yizhe building, Yuquan road, Nanshan
Shenzhen 518051 CN
Other 510(k) Applications for this Company
|
Contact |
Toki Wu
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 |
07/10/2017 |
Decision Date |
09/21/2017 |
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 |
|