
Truly Instrument Co., Ltd.
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TRYLY AUTOMATIC WRIST BLOOD PRESSURE MONITOR is an FDA 510(k)-cleared medical device (K113085) manufactured by Truly Instrument Co., Ltd.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 11, 2012. Regulation: 8.