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Blease Medical Equipment , Ltd.
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BLEASE SIRIUS ANESTHESIA SYSTEM, MODELS 3000 AND 2000 is an FDA 510(k)-cleared medical device (K041430) manufactured by Blease Medical Equipment , Ltd.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 6, 2004. Regulation: 8.