FDA 510(k) Application Details - K020929

Device Classification Name	System, X-Ray, Tomography, Computed   More FDA Info for this Device
510(K) Number	K020929
Device Name	System, X-Ray, Tomography, Computed
Applicant	GE MEDICAL SYSTEMS 283 RUE DE LA MINIERE BP 34 BUC CEDEX 78533 FR Other 510(k) Applications for this Company
Regulation Number	892.1750   More FDA Info for this Regulation Number
Classification Product Code	JAK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/22/2002
Decision Date	04/03/2002
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