FDA 510(k) Application Details - K052942

Device Classification Name	System, Image Processing, Radiological   More FDA Info for this Device
510(K) Number	K052942
Device Name	System, Image Processing, Radiological
Applicant	NEC-MITSUBISHI ELECTRIC VISUAL SYSTEMS CORP. 4-13-23 SHIBAURA MINATO-KU, TOKYO 108-0023 JP Other 510(k) Applications for this Company
Contact	SHUICHI KINO Other 510(k) Applications for this Contact
Regulation Number	892.2050   More FDA Info for this Regulation Number
Classification Product Code	LLZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/20/2005
Decision Date	12/27/2005
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	Y
Expedited Review