FDA 510(k) Application Details - K960839

Device Classification Name	Digitizer, Image, Radiological   More FDA Info for this Device
510(K) Number	K960839
Device Name	Digitizer, Image, Radiological
Applicant	CANNON U.S.A., INC. ONE CANNON PLAZA LAKE SUCCESS, NY 11042 US Other 510(k) Applications for this Company
Contact	GLEN IMPAL 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	02/26/1996
Decision Date	12/18/1996
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