ENDO-LASE CD40 FOR OTORHINOLARYNGOLOGY

ENDO-LASE CD40 FOR OTORHINOLARYNGOLOGY is an FDA 510(k)-cleared medical device (K853902) manufactured by Endo Lase, Inc.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 8, 1986. Regulation: 8.