FDA 510(k) Applications Submitted by Therapixel

FDA 510(k) Number Submission Date Device Name Applicant
K243679 11/29/2024 MammoScreen« (4) Therapixel
K240301 02/01/2024 MammoScreen« (3) Therapixel
K211541 05/19/2021 MammoScreen 2.0 Therapixel
K241561 05/31/2024 MammoScreen BD Therapixel
K192854 10/04/2019 MammoScreen Therapixel


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