
Nihon Seimitsu Sokki Co., Ltd.
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MODEL DS-1901 DIGITAL BLOOD PRESSURE MONITOR is an FDA 510(k)-cleared medical device (K050697) manufactured by Nihon Seimitsu Sokki 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 March 24, 2005. Regulation: 8.