Intertape Polymer Inc., Type 1 Bismuth Process Indicator Steam Sterilization Tape

Intertape Polymer Inc., Type 1 Bismuth Process Indicator Steam Sterilization Tape is an FDA 510(k)-cleared medical device (K191741) manufactured by Intertape Polymer, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 1, 2019. Regulation: 8.