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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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