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Philips Medical Systems, Inc.
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M2376A DEVICELINK SYSTEM, MODEL M2376A is an FDA 510(k)-cleared medical device (K014181) manufactured by Philips Medical Systems, 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 January 14, 2002. Regulation: 8.