
Endo Lase, Inc.
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ND: YAGLASER FOR PALLIATIVE TREAT OF OBSTRUCTION is an FDA 510(k)-cleared medical device (K852507) 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 July 4, 1985. Regulation: 8.

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