FDA 510(k) Application Details - K955000

Device Classification Name	System, Digital Image Communications, Radiological   More FDA Info for this Device
510(K) Number	K955000
Device Name	System, Digital Image Communications, Radiological
Applicant	CERNER CORP. 2800 ROCKCREEK PKWY. KANSAS CITY, MO 64117 US Other 510(k) Applications for this Company
Contact	PAUL A HELMUT Other 510(k) Applications for this Contact
Regulation Number	892.2020   More FDA Info for this Regulation Number
Classification Product Code	LMD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/01/1995
Decision Date	01/26/1996
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