LCX CHLAMYDIA TRACHOMATIS ASSAY

LCX CHLAMYDIA TRACHOMATIS ASSAY is an FDA 510(k)-cleared medical device (K934622) manufactured by Abbott Laboratories. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 7, 1995. Regulation: 8.