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Nihon Kohden Corp.
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GF-210R MULTI-GAS MODULE FOR NOHON KOHDEN BEDSIDE MONITORS is an FDA 510(k)-cleared medical device (K110594) manufactured by Nihon Kohden Corp.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 27, 2011. Regulation: 8.