
E. R. Squibb & Sons, Inc.
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ACTIVE-LIFE is an FDA 510(k)-cleared medical device (K780454) manufactured by E. R. Squibb & Sons, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 20, 1978. Regulation: 8.