HSV IN SITU DNA PROBE HYBRIDIZATION TEST KIT

HSV IN SITU DNA PROBE HYBRIDIZATION TEST KIT is an FDA 510(k)-cleared medical device (K911345) manufactured by Diagnostic Hybrids, Inc.. This device is classified under the Microbiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 16, 1991. Regulation: 8.