
Elmed, Inc.
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ELMED ESU 300 M/M AND DIGITAL is an FDA 510(k)-cleared medical device (K932938) manufactured by Elmed, 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 May 1, 1994. Regulation: 8.