
Drg Intl., Inc.
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ENZYME IMMUNOASSAY FOR THE DETECTION OF SALIVARY 17-A-HYDROXYPROGESTERONE is an FDA 510(k)-cleared medical device (K062534) manufactured by Drg Intl., Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 28, 2008. Regulation: 8.