FDA 510(k) Applications Submitted by SOURCE-RAY, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K133959 12/24/2013 PODIATRY X-RAY SYSTEM SOURCE-RAY, INC.
K030494 02/19/2003 SR-130 SOURCE-RAY, INC.
K090655 03/11/2009 PORTABLE X-RAY SYSTEM, MODEL POWERMAX 1260 SOURCE-RAY, INC.
K071392 05/18/2007 PXS-810, PODIATRY X-RAY SYSTEM SOURCE-RAY, INC.
K052001 07/25/2005 MODEL SR-115 PORTABLE X-RAY SYSTEM SOURCE-RAY, INC.
K062472 08/24/2006 OPTIONAL REMOTE CONTROL, MODEL RC-115, FOR PORTABLE X-RAY SYSTEM, MODEL SR-115 SOURCE-RAY, INC.
K163063 11/02/2016 UC-5000 Mobile X-Ray SOURCE-RAY, INC.
K043062 11/05/2004 MODEL SR-130-D PORTABLE DIGITAL X-RAY SYSTEM SOURCE-RAY, INC.


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