
KARL STORZ Endoscopy-America, Inc.
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KSEA CLEARVISION II, MODEL 40334120 is an FDA 510(k)-cleared medical device (K072410) manufactured by KARL STORZ Endoscopy-America, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 8, 2008. Regulation: 8.