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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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