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Mediaid, Inc.
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MEDIAID PULSE OXIMETER M30 AND M34 is an FDA 510(k)-cleared medical device (K071610) manufactured by Mediaid, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 4, 2007. Regulation: 8.