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KARL STORZ Endoscopy-America, Inc.
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KSEA ELECTRONIC CO2 ENDOFLATOR LC, MODEL 26430320-1 is an FDA 510(k)-cleared medical device (K080852) manufactured by KARL STORZ Endoscopy-America, Inc.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 29, 2009. Regulation: 8.

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