SCANLAN HEIFETZ ANEURYSM ELGILOY CLIP SYSTEM

SCANLAN HEIFETZ ANEURYSM ELGILOY CLIP SYSTEM is an FDA 510(k)-cleared medical device (K960372) manufactured by Scanlan Intl., Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 25, 1996. Regulation: 8.