FDA 510(k) Application Details - K111019

Device Classification Name	System, Image Processing, Radiological   More FDA Info for this Device
510(K) Number	K111019
Device Name	System, Image Processing, Radiological
Applicant	NEMARIS INC 1425 K STREET N.W. 11TH FLOOR WASHINGTON, DC 20005 US Other 510(k) Applications for this Company
Contact	KEITH A BARRITT 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	04/12/2011
Decision Date	09/30/2011
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