FDA 510(k) Application Details - K032280

Device Classification Name	System, X-Ray, Mobile   More FDA Info for this Device
510(K) Number	K032280
Device Name	System, X-Ray, Mobile
Applicant	SIEMENS AG 51 VALLEY STREAM PARKWAY MALVERN, PA 19355 US Other 510(k) Applications for this Company
Contact	NEALIE HARTMAN Other 510(k) Applications for this Contact
Regulation Number	892.1720   More FDA Info for this Regulation Number
Classification Product Code	IZL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/24/2003
Decision Date	09/10/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review