FDA 510(k) Applications Submitted by Karen Smith

FDA 510(k) Number Submission Date Device Name Applicant
K211979 06/25/2021 Lumenis Y&R Laser System Lumenis Inc.
K232903 09/18/2023 Legend X Platform Pollogen Ltd
K243217 10/03/2024 Legend X Desktop System Pollogen Ltd.
K233766 11/24/2023 Geneo X Elite Pollogen Ltd.


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