
Amsco Sterile Recoveries, Inc.
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REUSABLE LIQUIDPROOF BOOTIE is an FDA 510(k)-cleared medical device (K925815) manufactured by Amsco Sterile Recoveries, 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 8, 1993. Regulation: 8.