INBODY 770, INBODY 570, INBODY S10, INBODY H20/INBODY H20(B)

INBODY 770, INBODY 570, INBODY S10, INBODY H20/INBODY H20(B) is an FDA 510(k)-cleared medical device (K123228) 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 March 7, 2013. Regulation: 8.