FDA 510(k) Application Details - K230768

Device Classification Name	System, Imaging, Pulsed Doppler, Ultrasonic   More FDA Info for this Device
510(K) Number	K230768
Device Name	System, Imaging, Pulsed Doppler, Ultrasonic
Applicant	Shenzhen Mindray Bio-Medical Electronics Co.,LTD Keji 12th Road South, Hi-tech Industrial Park Shenzhen 518057 CN Other 510(k) Applications for this Company
Contact	Tang Jing 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	03/20/2023
Decision Date	06/09/2023
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