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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