FDA 510(k) Applications Submitted by PENTRON CLINICAL

FDA 510(k) Number Submission Date Device Name Applicant
K120013 01/03/2012 TEMPSPAN CLEAR MATRIX PENTRON CLINICAL
K130920 04/03/2013 CORRECT PLUS 1 PENTRON CLINICAL
K111431 05/23/2011 B1P ADHESIVE PENTRON CLINICAL
K102703 09/20/2010 BUILD-IT TOTAL CORE PENTRON CLINICAL


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