STERITEC AUTOCLAVE TAPES, MODEL CI122 & CI1234

STERITEC AUTOCLAVE TAPES, MODEL CI122 & CI1234 is an FDA 510(k)-cleared medical device (K001649) manufactured by Steritec Products, 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 June 22, 2000. Regulation: 8.