
Global Endoscopy, Inc.
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GYNECOLOGICAL LAPAROSCOPES is an FDA 510(k)-cleared medical device (K003805) manufactured by Global Endoscopy, 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 July 21, 2001. Regulation: 8.

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