HERPTRAN CONCENTRATE

HERPTRAN CONCENTRATE is an FDA 510(k)-cleared medical device (K900713) manufactured by E.I. Dupont DE Nemours & Co., 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 May 10, 1990. Regulation: 8.