FDA 510(k) Application Details - K022337

Device Classification Name	System, X-Ray, Mobile   More FDA Info for this Device
510(K) Number	K022337
Device Name	System, X-Ray, Mobile
Applicant	SIEMENS MEDICAL SOLUTIONS USA, INC. 186 WOOD AVENUE SOUTH ISELIN, NJ 08830 US Other 510(k) Applications for this Company
Contact	AMY SHAW HOSLER 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	07/18/2002
Decision Date	08/13/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review