INDIRECT FLUORESCENT ASSAY FOR HERPES SIMPLEX 1

INDIRECT FLUORESCENT ASSAY FOR HERPES SIMPLEX 1 is an FDA 510(k)-cleared medical device (K905608) manufactured by Stellar Bio Systems, 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 November 6, 1991. Regulation: 8.