FDA 510(k) Applications Submitted by GLIDEWELL LABORATORIES

FDA 510(k) Number Submission Date Device Name Applicant
K060104 01/13/2006 PRISMATIK CLINICAL ZIRCONIA GLIDEWELL LABORATORIES
K050144 01/24/2005 PRISMATIK CERAMIC GLIDEWELL LABORATORIES
K972424 06/27/1997 SILENTNITE GLIDEWELL LABORATORIES


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