FDA 510(k) Application Details - K090655

Device Classification Name	System, X-Ray, Mobile   More FDA Info for this Device
510(K) Number	K090655
Device Name	System, X-Ray, Mobile
Applicant	SOURCE-RAY, INC. 167 KEYLAND CT. BOHEMIA, NY 11716 US Other 510(k) Applications for this Company
Contact	RAY MANEZ Other 510(k) Applications for this Contact
Regulation Number	892.1720   More FDA Info for this Regulation Number
Classification Product Code	IZL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/11/2009
Decision Date	07/14/2009
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review