
London Diagnostics, Inc.
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LONDON DIAGNOSTICS LUMATAG(R) HGH CHEM IMMUN ASSAY is an FDA 510(k)-cleared medical device (K912858) manufactured by London Diagnostics, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 29, 1991. Regulation: 8.