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

FDA 510(k) Number Applicant Device Name Decision Date
K191194 Carl Zeiss Meditec, Inc CLARUS 06/25/2019
K181444 Carl Zeiss Meditec, Inc. CLARUS 01/10/2019
K243878 Carl Zeiss Meditec, Inc. CLARUS (700) 04/17/2025


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