ANTI-RESPIRATORY SYNCYTIAL VIRUS ANTIBODY TEST

ANTI-RESPIRATORY SYNCYTIAL VIRUS ANTIBODY TEST is an FDA 510(k)-cleared medical device (K882687) manufactured by Gull Laboratories, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 29, 1988. Regulation: 8.