
Trinity Laboratories, Inc.
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CAT.#40100, 40102, 40104 & 40106 YANKAUER SUCT INT is an FDA 510(k)-cleared medical device (K921464) manufactured by Trinity Laboratories, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 4, 1992. Regulation: 8.