
E. R. Squibb & Sons, Inc.
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STOMAHESIVE POWDER is an FDA 510(k)-cleared medical device (K792382) 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 December 19, 1979. Regulation: 8.