DSL ACTIVE NON-EXTRACTION IGF-I ELISA

DSL ACTIVE NON-EXTRACTION IGF-I ELISA is an FDA 510(k)-cleared medical device (K971353) 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 11, 1997. Regulation: 8.