FDA 510(k) Application Details - K103448

Device Classification Name	System, X-Ray, Stationary   More FDA Info for this Device
510(K) Number	K103448
Device Name	System, X-Ray, Stationary
Applicant	GE MEDICAL SYSTEMS, LLC 3000 N GRANDVIEW BLVD. WAUKESHA, WI 53188 US Other 510(k) Applications for this Company
Contact	JOHN L SCHMIDT Other 510(k) Applications for this Contact
Regulation Number	892.1680   More FDA Info for this Regulation Number
Classification Product Code	KPR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/24/2010
Decision Date	08/12/2011
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	N
Expedited Review