FDA 510(k) Application Details - K113701

Device Classification Name	System, Image Processing, Radiological   More FDA Info for this Device
510(K) Number	K113701
Device Name	System, Image Processing, Radiological
Applicant	MEVIS MEDICAL SOLUTIONS AG N27 W24075 PAUL COURT SUITE 100 PEWAUKEE, WI 53072 US Other 510(k) Applications for this Company
Contact	THOMAS E TYNES 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	12/16/2011
Decision Date	02/16/2012
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