DSL ACTIVE IFGBP-3 ELISA

DSL ACTIVE IFGBP-3 ELISA is an FDA 510(k)-cleared medical device (K951707) 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 9, 1995. Regulation: 8.