FDA 510(k) Application Details - K070244

Device Classification Name	System, Image Processing, Radiological   More FDA Info for this Device
510(K) Number	K070244
Device Name	System, Image Processing, Radiological
Applicant	SENTINELLE MEDICAL, INC. 3080 YONGE STREET SUITE 6020 TORONTO, ONTARIO M4N 3N1 CA Other 510(k) Applications for this Company
Contact	STEPHEN LEUNG 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	01/25/2007
Decision Date	02/09/2007
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