RESP. SYNCYTIAL-FA LABELLED PRESERUM

RESP. SYNCYTIAL-FA LABELLED PRESERUM is an FDA 510(k)-cleared medical device (K770808) manufactured by Flow Laboratories, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 19, 1977. Regulation: 8.