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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