FDA 510(k) Application Details - K201995

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