FDA 510(k) Applications Submitted by CALVIN D OSTLER

FDA 510(k) Number Submission Date Device Name Applicant
K100474 02/18/2010 QUICKLASEDUAL+, QUICKLASE810, QUICKLASE810, QUICKLASE980, QUICKLASE980 MODEL: 3W,5W,3W,5W QUICKLASE LIMITED
K970637 02/20/1997 ACCUCURE 1000 LASERMED, INC.
K992061 06/18/1999 PULSTAR LASERMED, INC.
K072995 10/23/2007 TWINWAVE DENTAL LASER, TIDALWAVE 810 DENTAL LASER, TIDALWAVE 980 DENTAL LASER LUMEN DEVELOPMENT AND MANUFACTURING, INC.
K964486 11/08/1996 ACCUCURE 3000 LASERMED, INC.


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