L.A.S.E.R., Inc. - FDA 510(k) Cleared Devices

L.A.S.E.R., Inc. has 14 FDA 510(k) cleared medical devices. Based in Chicago, US.

Historical record: 14 cleared submissions from 1985 to 1998. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by L.A.S.E.R., Inc. Filter by specialty or product code using the sidebar.