VIDAS CHLAMYDIA ASSAY VITEK IMMUNDIAG ASSAY SYST

VIDAS CHLAMYDIA ASSAY VITEK IMMUNDIAG ASSAY SYST is an FDA 510(k)-cleared medical device (K905787) manufactured by Vitek Systems, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 28, 1991. Regulation: 8.