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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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