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Phamatech, Inc.
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PHARMATECH MENOPAUSE CHECK, MODELS 9111 AND 9112 is an FDA 510(k)-cleared medical device (K040575) manufactured by Phamatech, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 19, 2004. Regulation: 8.