FDA 510(k) Application Details - K160790

Device Classification Name	System, Imaging, Pulsed Doppler, Ultrasonic   More FDA Info for this Device
510(K) Number	K160790
Device Name	System, Imaging, Pulsed Doppler, Ultrasonic
Applicant	Edan Instruments Inc 3/F-B, Nanshan Medical Equipments Park, Nanhai Rd 1019# Shenzhen 518067 CN Other 510(k) Applications for this Company
Contact	Queena Chen 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	03/22/2016
Decision Date	04/04/2016
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	Y
Expedited Review