FDA 510(k) Application Details - K132341

Device Classification Name	System, Imaging, Pulsed Doppler, Ultrasonic   More FDA Info for this Device
510(K) Number	K132341
Device Name	System, Imaging, Pulsed Doppler, Ultrasonic
Applicant	SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD MINDRAY BLDG. KEJI 12TH RD S. HI-TECH INDUSTRIAL PARK NANSHAN, SHENZHEN 518057 CN Other 510(k) Applications for this Company
Contact	ZHAI PEI 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	07/26/2013
Decision Date	08/15/2013
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