
London Diagnostics, Inc.
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LUMATAG(TM) PROLACTIN CHEMILUMINES. IMMUNO. ASSAY is an FDA 510(k)-cleared medical device (K880296) 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 March 23, 1988. Regulation: 8.