FDA 510(k) Application Details - K062163

Device Classification Name	System, Image Processing, Radiological   More FDA Info for this Device
510(K) Number	K062163
Device Name	System, Image Processing, Radiological
Applicant	MIMVISTA CORP. 25200 CHAGRIN BLVD. SUITE 200 CLEVELAND, OH 44122 US Other 510(k) Applications for this Company
Contact	PETER SIMMELINK 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	07/28/2006
Decision Date	09/22/2006
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