
CooperSurgical, Inc.
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Endosee System is an FDA 510(k)-cleared medical device (K200038) manufactured by CooperSurgical, 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 February 4, 2020. Regulation: 8.

Ansell
SKU MSC846624

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SKU VM-1270031