STERICHEK(TM) RESIDUAL PEROXIDE REAGENT STRPS

STERICHEK(TM) RESIDUAL PEROXIDE REAGENT STRPS is an FDA 510(k)-cleared medical device (K974798) manufactured by Environmental Test Systems, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 19, 1998. Regulation: 8.