
Resmed Germany, Inc.
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APNEALINK PLUS, MODEL: 22328 is an FDA 510(k)-cleared medical device (K083575) manufactured by Resmed Germany, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 18, 2009. Regulation: 8.