
Beacon Laboratories, Inc.
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BEAMER 1,2,4,6, AND 8 is an FDA 510(k)-cleared medical device (K903724) manufactured by Beacon Laboratories, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 27, 1990. Regulation: 8.