
Diagnostic Systems Laboratories, Inc.
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ACTIVE DEHYDROEPIANDROSTERONE (DHEA)(DSL 9000) is an FDA 510(k)-cleared medical device (K935014) manufactured by Diagnostic Systems Laboratories, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 8, 1994. Regulation: 8.