FDA 510(k) Application Details - K962589

Device Classification Name	System, Image Processing, Radiological   More FDA Info for this Device
510(K) Number	K962589
Device Name	System, Image Processing, Radiological
Applicant	AURORA TECHNOLOGY, INC. 10560 WAYZATA BLVD. MINNEAPOLIS, MN 55305 US Other 510(k) Applications for this Company
Contact	C. PAUL PESEK 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	07/02/1996
Decision Date	09/20/1996
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