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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