FDA 510(k) Application Details - K140899

Device Classification Name	System, Imaging, Pulsed Echo, Ultrasonic   More FDA Info for this Device
510(K) Number	K140899
Device Name	System, Imaging, Pulsed Echo, Ultrasonic
Applicant	HALO MEDICAL TECHNOLOGIES, LLC 1805 FOULK ROAD, SUITE G WILMINGTON, DE 19810 US Other 510(k) Applications for this Company
Contact	JENNIFER L KINNEY Other 510(k) Applications for this Contact
Regulation Number	892.1560   More FDA Info for this Regulation Number
Classification Product Code	IYO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/08/2014
Decision Date	05/05/2014
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