FDA 510(k) Application Details - K111833

Device Classification Name	System, Image Processing, Radiological   More FDA Info for this Device
510(K) Number	K111833
Device Name	System, Image Processing, Radiological
Applicant	DIAGNOSOFT, INC. 49 PLAIN STREET NORTH ATTLEBORO, MA 02760 US Other 510(k) Applications for this Company
Contact	JEFFREY ROBERTS 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	06/28/2011
Decision Date	09/21/2011
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