ATTACHABLE LANZ (TENTATIVE)

ATTACHABLE LANZ (TENTATIVE) is an FDA 510(k)-cleared medical device (K885216) manufactured by Mallinckroot, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 13, 1989. Regulation: 8.