VIDAS RESPIRATORY SYNCYTIAL VIRUS (RSV) ASSAY

VIDAS RESPIRATORY SYNCYTIAL VIRUS (RSV) ASSAY is an FDA 510(k)-cleared medical device (K896097) 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 February 25, 1990. Regulation: 8.