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Biospace Corporation Limited
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BIOSPACE BODY COMPOSITION ANALYZERS, MODEL INBODY 230 is an FDA 510(k)-cleared medical device (K062603) manufactured by Biospace Corporation Limited. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 14, 2007. Regulation: 8.