FDA 510(k) Application Details - K093688

Device Classification Name	More FDA Info for this Device
510(K) Number	K093688
Device Name	CANON, MODEL URS-50RF
Applicant	VIRTUAL IMAGING, INC. 8726 FERRARA CT NAPLES, FL 34114 US Other 510(k) Applications for this Company
Contact	DANIEL KAMM Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	OWB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/30/2009
Decision Date	02/04/2010
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