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Welch Allyn, Inc.
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WELCH ALLYN INSTRUMENT INTERFACE MODULE is an FDA 510(k)-cleared medical device (K001265) manufactured by Welch Allyn, 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 July 12, 2000. Regulation: 8.