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FDA 510(k) Applications Submitted by LightScalpel LLC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K132661
08/26/2013
LIGHTSCALPEL
LIGHTSCALPEL LLC
K123037
09/28/2012
LIGHTSCALPEL
LIGHTSCALPEL LLC
K173827
12/18/2017
LightScalpel
LightScalpel LLC
K121471
05/18/2012
LIGHTSCALPEL FAMILY OF HANDPIECE TIPS FOR CO2 SURGICAL LASERS
LIGHTSCALPEL LLC
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