FDA 510(k) Application Details - K131137

Device Classification Name	System, Image Processing, Radiological   More FDA Info for this Device
510(K) Number	K131137
Device Name	System, Image Processing, Radiological
Applicant	JVC KENWOOD CORPORATION 300-OYA UEDA-SHI NAGANO-KEN 386-0192 JP Other 510(k) Applications for this Company
Contact	TSUKASA TASHIRO 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	04/23/2013
Decision Date	07/18/2013
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