FDA 510(k) Applications Submitted by Hans-Joachim Miesner

FDA 510(k) Number Submission Date Device Name Applicant
K230858 03/29/2023 QUATERA 700 Carl Zeiss Meditec AG
K211346 05/03/2021 BLUE 400 Carl Zeiss Meditec AG
K231676 06/09/2023 CALLISTO eye Carl Zeiss Meditec AG
K212241 07/19/2021 QUATERA 700 Carl Zeiss Meditec AG


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