FDA 510(k) Applications Submitted by CLINICON CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K970143 01/15/1997 C4 CLINICON CORP.
K962242 06/11/1996 SURESCAN CLINICON CORP.
K964831 12/02/1996 SURESCAN CLINICON CORP.
K121580 05/30/2012 SURELASE CO2 LASER SYSTEM CLINICON CORP.
K992472 07/26/1999 SUREGUIDE CO2 LASER BEAM DELIVERY SYSTEM CLINICON CORP.
K983463 10/01/1998 SURECAUT DIAMOND LASER KNIFE CLINICON CORP.
K063698 12/13/2006 CO2 LASER SYSTEM, MODEL C-LAS CLINICON CORP.
K014048 12/07/2001 CLINICON UNIVERSAL WAVEGUIDE HANDPIECE AND FIBER TIPS CLINICON CORP.
K014236 12/26/2001 CLINICON WAVEGUIDE PLATFORM WITH INTERCONNECT FOR LUXAR ACCESSORIES CLINICON CORP.


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