FDA 510(k) Applications for Medical Device Product Code "PPW"

FDA 510(k) Number Applicant Device Name Decision Date
K213230 Etiometry, Inc. T3 Platform Software 06/22/2022
K223578 Etiometry, Inc. T3 Platform software 07/07/2023
K173929 Flashback Technologies, Inc. CipherOx CRI M1 07/24/2018
DEN160020 Flashback Technologies, Inc. CipherOx CRI Tablet 12/21/2016
K213255 Flashback Technologies, Inc. CipherOx CRI Tablet 06/17/2022


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