FDA 510(k) Applications Submitted by MARK D BROWN

FDA 510(k) Number Submission Date Device Name Applicant
K240535 02/26/2024 Digital ClarusScope System; Digital NeuroPEN System Clarus Medical, LLC
K010194 01/22/2001 COMFOR-CLINER RECLINER CARE, INC.
K200925 04/07/2020 Clarus Peel-Away Introducer Sheath Clarus Medical, LLC
K223615 12/05/2022 Digital ClarusScope System, Digital NeuroPEN System Clarus Medical, LLC


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