FDA 510(k) Applications Submitted by NAAMA JACOBY

FDA 510(k) Number Submission Date Device Name Applicant
K170060 01/06/2017 M22 and ResurFx Systems LUMENIS, LTD.
K162837 10/11/2016 Smart Laser Indirect Ophthalmoscope (LIO); Laser delivery device for Lumenis Novus Spectra Laser System, Lumenis Vision One Laser System, and Lumenis Smart532Ö Laser System LUMENIS LTD


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