RAPID DIAGNOSTIC SYSTEM FOR CHLAMYDIA TRACHOMATIS

RAPID DIAGNOSTIC SYSTEM FOR CHLAMYDIA TRACHOMATIS is an FDA 510(k)-cleared medical device (K871878) manufactured by Gen-Probe, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 27, 1987. Regulation: 8.