FDA 510(k) Application Details - K050846

Device Classification Name	System, Image Processing, Radiological   More FDA Info for this Device
510(K) Number	K050846
Device Name	System, Image Processing, Radiological
Applicant	THE MEDIPATTERN CORPORATION 2300 SHEPPARD AVE W SUITE 204 TORONTO, ON M9M 3A4 CA Other 510(k) Applications for this Company
Contact	PATRICIA A MILBANK 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	04/04/2005
Decision Date	05/26/2005
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	N
Expedited Review