
Davis & Geck, Inc.
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APPOSE DISPOS. SKIN STAPLER W/AUTO is an FDA 510(k)-cleared medical device (K840178) manufactured by Davis & Geck, 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 March 4, 1984. Regulation: 8.

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