HEIFETZ ANEURYSM CLIP, LMM BLADE

HEIFETZ ANEURYSM CLIP, LMM BLADE is an FDA 510(k)-cleared medical device (K790413) manufactured by Edward Weck, 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 March 15, 1979. Regulation: 8.