FDA 510(k) Application Details - K130278

Device Classification Name	System, Image Processing, Radiological   More FDA Info for this Device
510(K) Number	K130278
Device Name	System, Image Processing, Radiological
Applicant	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. 595 MINER RD CLEVELAND, OH 44143 US Other 510(k) Applications for this Company
Contact	SUSAN QUICK 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	02/05/2013
Decision Date	05/29/2013
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