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FDA 510(k) Applications Submitted by Ken Koster
FDA 510(k) Number
Submission Date
Device Name
Applicant
K222676
09/06/2022
Ceevra Reveal 3
Ceevra, Inc.
K233568
11/06/2023
Ceevra Reveal 3+
Ceevra, Inc.
K243933
12/20/2024
Ceevra Reveal 3+
Ceevra, Inc.
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