FDA 510(k) Application Details - K042484

Device Classification Name	Digitizer, Image, Radiological   More FDA Info for this Device
510(K) Number	K042484
Device Name	Digitizer, Image, Radiological
Applicant	NAI TECHNOLOGY PRODUCTS 1342-D NORTH BENSON AVENUE UPLAND, CA 91786 US Other 510(k) Applications for this Company
Contact	ROBERT E JOHNSON Other 510(k) Applications for this Contact
Regulation Number	892.2030   More FDA Info for this Regulation Number
Classification Product Code	LMA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/13/2004
Decision Date	10/20/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review