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.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact