FDA 510(k) Application Details - K122697

Device Classification Name	System, X-Ray, Mobile   More FDA Info for this Device
510(K) Number	K122697
Device Name	System, X-Ray, Mobile
Applicant	JOB CORPORATION 1411 W. 190TH STREET SUITE 120 GARDENA, CA 92048 US Other 510(k) Applications for this Company
Contact	TAKAHIRO HARUYAMA Other 510(k) Applications for this Contact
Regulation Number	892.1720   More FDA Info for this Regulation Number
Classification Product Code	IZL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/04/2012
Decision Date	10/05/2012
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