FDA 510(k) Applications Submitted by SOURCE PRODUCTION & EQUIPMENT CO., INC.

FDA 510(k) Number Submission Date Device Name Applicant
K090366 02/13/2009 SPEC MODEL M-31 SOURCE PRODUCTION & EQUIPMENT CO., INC.
K052947 10/20/2005 SOURCE PRODUCTION & EQUIPMENT CO, INC., MODEL M-19 IR-192 BRACHYTHERAPY SOURCE SOURCE PRODUCTION & EQUIPMENT CO., INC.
K132969 09/23/2013 SPEC MODEL M15 SOURCE PRODUCTION & EQUIPMENT CO., INC.


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