FDA 510(k) Application Details - K992066

Device Classification Name	System, X-Ray, Stationary   More FDA Info for this Device
510(K) Number	K992066
Device Name	System, X-Ray, Stationary
Applicant	GE MEDICAL SYSTEMS 3000 N GRANDVIEW BLVD. W-709 WAUKESHA, WI 53188 US Other 510(k) Applications for this Company
Contact	LARRY A KROGER 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	06/18/1999
Decision Date	08/30/1999
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