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FDA 510(k) Applications Submitted by Pollogen Ltd.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K203665
12/16/2020
STOP U Model UXV Device
Pollogen Ltd.
K182774
10/01/2018
STOP U (Packed Black USA), STOP U (Packed White USA)
Pollogen Ltd.
K173503
11/13/2017
Pollogen Legend System
Pollogen Ltd.
K220322
02/03/2022
Pollogen STOP U Model UXV Device
Pollogen Ltd.
K171359
05/09/2017
Pollogen Legend+ System
Pollogen Ltd.
K220124
01/18/2022
YandR System, VoluDerm Handpiece, VoluDerm Tips
Pollogen Ltd.
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