FDA 510(k) Application Details - K051133

Device Classification Name	More FDA Info for this Device
510(K) Number	K051133
Device Name	ARCADIS AVANTIC
Applicant	SIEMENS MEDICAL SOLUTIONS USA, INC. 51 VALLEY STREAM PARKWAY, E-50 MALVERN, PA 19355 US Other 510(k) Applications for this Company
Contact	MICHAEL J ANDREWS Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	OXO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/03/2005
Decision Date	06/01/2005
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