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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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