
Clarus Medical, LLC
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Clarus Peel-Away Introducer Sheath is an FDA 510(k)-cleared medical device (K200925) manufactured by Clarus Medical, LLC. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 17, 2021. Regulation: 8.

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