Clinicon Corp. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
FDA 510(k) Regulatory Record - Clinicon Corp. General & Plastic Surgery ✕
9 devices
Cleared
Sep 25, 2012
SURELASE CO2 LASER SYSTEM
General & Plastic Surgery
118d
Cleared
Mar 02, 2007
CO2 LASER SYSTEM, MODEL C-LAS
General & Plastic Surgery
79d
Cleared
Mar 26, 2002
CLINICON WAVEGUIDE PLATFORM WITH INTERCONNECT FOR LUXAR ACCESSORIES
General & Plastic Surgery
90d
Cleared
Feb 11, 2002
CLINICON UNIVERSAL WAVEGUIDE HANDPIECE AND FIBER TIPS
General & Plastic Surgery
66d
Cleared
Sep 08, 1999
SUREGUIDE CO2 LASER BEAM DELIVERY SYSTEM
General & Plastic Surgery
44d
Cleared
Dec 11, 1998
SURECAUT DIAMOND LASER KNIFE
General & Plastic Surgery
71d
Cleared
Oct 29, 1997
C4
General & Plastic Surgery
287d
Cleared
Aug 08, 1997
SURESCAN
General & Plastic Surgery
249d
Cleared
Sep 03, 1996
SURESCAN
General & Plastic Surgery
84d