FDA 510(k) Application Details - K093146

Device Classification Name	System, X-Ray, Tomography, Computed   More FDA Info for this Device
510(K) Number	K093146
Device Name	System, X-Ray, Tomography, Computed
Applicant	VERAN MEDICAL TECHNOLOGIES, INC. 5743 WEST PARK AVE ST. LOUIS, MO 63110 US Other 510(k) Applications for this Company
Contact	SCOTT WRIGHTSTONE Other 510(k) Applications for this Contact
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	10/05/2009
Decision Date	11/30/2009
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