FDA 510(k) Applications Submitted by Kelley Richardt

FDA 510(k) Number Submission Date Device Name Applicant
K161395 05/19/2016 SPEC Model M13 Source Production and Equipment Co.,Inc.
K161396 05/19/2016 SPEC Model M23 Source Production and Equipment Co.,Inc.
K162573 09/15/2016 Source Production & Equipment Co., Inc. Model M14 192Iridium Brachytherapy Source SOURCE PRODUCTION AND EQUIPMENT CO., INC.
K132969 09/23/2013 SPEC MODEL M15 SOURCE PRODUCTION & EQUIPMENT CO., INC.


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