
Genicon, LC
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INSUFFLATION NEEDLE- 120MM, MODEL 900-200 is an FDA 510(k)-cleared medical device (K993625) manufactured by Genicon, LC. 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 June 19, 2000. Regulation: 8.

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