
American Bentley
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ELECTROSURGICAL LATERAL RELEASE PROBE MOD ALR-100 is an FDA 510(k)-cleared medical device (K852683) manufactured by American Bentley. 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 August 11, 1985. Regulation: 8.