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FDA 510(k) Applications Submitted by GERALD PALECKI
FDA 510(k) Number
Submission Date
Device Name
Applicant
K121580
05/30/2012
SURELASE CO2 LASER SYSTEM
CLINICON CORP.
K121471
05/18/2012
LIGHTSCALPEL FAMILY OF HANDPIECE TIPS FOR CO2 SURGICAL LASERS
LIGHTSCALPEL LLC
K992472
07/26/1999
SUREGUIDE CO2 LASER BEAM DELIVERY SYSTEM
CLINICON CORP.
K983463
10/01/1998
SURECAUT DIAMOND LASER KNIFE
CLINICON CORP.
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