FDA 510(k) Application Details - K121577

Device Classification Name	System, Imaging, Pulsed Doppler, Ultrasonic   More FDA Info for this Device
510(K) Number	K121577
Device Name	System, Imaging, Pulsed Doppler, Ultrasonic
Applicant	TOSHIBA MEDICAL SYSTEMS CORPORATION, JAPAN 2441 MICHELLE DR TUSTIN, CA 92780 US Other 510(k) Applications for this Company
Contact	CHARLEMAGNE CHUA 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	05/30/2012
Decision Date	06/22/2012
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