FDA 510(k) Application Details - K093371

Device Classification Name	System, Imaging, Pulsed Echo, Ultrasonic   More FDA Info for this Device
510(K) Number	K093371
Device Name	System, Imaging, Pulsed Echo, Ultrasonic
Applicant	DGH TECHNOLOGY, INC. 110 SUMMIT DR., SUITE B EXTON, PA 19341 US Other 510(k) Applications for this Company
Contact	M. LUTHER DETWEILER 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	10/29/2009
Decision Date	04/05/2010
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