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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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