
Rcx-Western, Inc.
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EPILATOR, BLEND-MODEL EB-200 & ET-1 is an FDA 510(k)-cleared medical device (K811503) manufactured by Rcx-Western, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 9, 1981. Regulation: 8.