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Atmos, Inc.
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ATMOS E 201 THORAX AND ATMOS S 201 THORAX is an FDA 510(k)-cleared medical device (K103042) manufactured by Atmos, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 14, 2011. Regulation: 8.