67-8006 DARLING-LINTON AORTIC TOURN.

67-8006 DARLING-LINTON AORTIC TOURN. is an FDA 510(k)-cleared medical device (K761161) manufactured by Codman & Shurtleff, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 5, 1976. Regulation: 8.