
Clarus Medical Systems, Inc.
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CLARUS SERIRS 2200 SEMI-RIGID ENDOSCOPE is an FDA 510(k)-cleared medical device (K924554) manufactured by Clarus Medical Systems, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 24, 1993. Regulation: 8.