
Selicor, Inc.
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SELICOR, MODELS A100 & D100 is an FDA 510(k)-cleared medical device (K020227) manufactured by Selicor, 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 July 29, 2002. Regulation: 8.