
Karl Storz Endoscopy
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KSEA CO2 ENDOFLATOR is an FDA 510(k)-cleared medical device (K963423) manufactured by Karl Storz Endoscopy. 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 May 26, 1997. Regulation: 8.

Ansell
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SKU VM-1270030

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SKU VM-1270031