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Beiersdorf, Inc.
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ANTI-EMBOLISM STOCKINGS, MODELS 71055-00000-02, 71057-00000-02, 71059-00000-02, 71064-00000-02 & 71065-00000-02 is an FDA 510(k)-cleared medical device (K090921) manufactured by Beiersdorf, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 17, 2009. Regulation: 8.

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