HUANG VEIN HOLDER, #21-8011

HUANG VEIN HOLDER, #21-8011 is an FDA 510(k)-cleared medical device (K771026) 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 June 19, 1977. Regulation: 8.