
Trinity Laboratories, Inc.
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CENTRAL VENOUS CATHETER, DRESSING CHANGE KIT, STER is an FDA 510(k)-cleared medical device (K920846) manufactured by Trinity Laboratories, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 31, 1992. Regulation: 8.