FDA 510(k) Application Details - K102390

Device Classification Name	System, Imaging, Pulsed Doppler, Ultrasonic   More FDA Info for this Device
510(K) Number	K102390
Device Name	System, Imaging, Pulsed Doppler, Ultrasonic
Applicant	SONOSITE,INC. 21919 30TH DRIVE SE. BOTHELL, WA 98021-3904 US Other 510(k) Applications for this Company
Contact	JESSICA R STENBERG 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	08/23/2010
Decision Date	11/19/2010
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