
Conmed Corporation
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AirSeal® dV Solution- AirSeal® Cannula Cap and AirSeal® Bifurcated Filtered Tube Set is an FDA 510(k)-cleared medical device (K211104) manufactured by Conmed 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 August 18, 2021. Regulation: 8.

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