
Healthonics, Inc.
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MEDRELIEF SE SERIES, MODELS SE-50, SE-100, SE-200, SE-300 is an FDA 510(k)-cleared medical device (K030998) manufactured by Healthonics, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 9, 2003. Regulation: 8.