
Endosec Corporation
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U-SCOPE 8000 SYSTEM WITH HSC+EMB CANNULA is an FDA 510(k)-cleared medical device (K132384) manufactured by Endosec Corporation. 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 July 1, 2014. Regulation: 8.

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