SHELL KRATON THERMO-PLASTIC RUBBER COMP.

SHELL KRATON THERMO-PLASTIC RUBBER COMP. is an FDA 510(k)-cleared medical device (K803069) manufactured by Warren E. Collins, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 21, 1980. Regulation: 8.