
Acrymed, Inc.
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ACRY ISLAND BORDER DRESSING, MODELS 2031, 2032, 2033 is an FDA 510(k)-cleared medical device (K992032) manufactured by Acrymed, Inc.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 18, 1999. Regulation: 8.

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