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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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