Device Classification Name |
System, Imaging, Pulsed Echo, Ultrasonic
More FDA Info for this Device |
510(K) Number |
K201995 |
Device Name |
System, Imaging, Pulsed Echo, Ultrasonic |
Applicant |
Mcube Technology Co., Ltd.
#803, 123, Bonghwasan-ro, Jungnang-gu
Seoul 02048 KR
Other 510(k) Applications for this Company
|
Contact |
Hye-Ri Choi
Other 510(k) Applications for this Contact |
Regulation Number |
892.1560
More FDA Info for this Regulation Number |
Classification Product Code |
IYO
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
Date Received |
07/20/2020 |
Decision Date |
08/19/2020 |
Decision |
SESE - SUBST EQUIV |
Classification Advisory Committee |
RA - Radiology |
Review Advisory Committee |
RA - Radiology |
Statement / Summary / Purged Status |
Summary |
Type |
Special |
Reviewed By Third Party |
N |
Expedited Review |
|