
London Diagnostics, Inc.
Free shipping on orders over $99 · 30-day returns
LUMATAG(TM) PROLACTIN DIAGNOSTIC KIT/MODIFICATION is an FDA 510(k)-cleared medical device (K904458) 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 October 11, 1990. Regulation: 8.