
Huntington Laboratories, Inc.
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FORMULATION HWS-256 EPA REG. NO. 47371-129 is an FDA 510(k)-cleared medical device (K953010) manufactured by Huntington Laboratories, Inc.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 10, 1995. Regulation: 8.

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