
Edward Weck, Inc.
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LM15(TM), CATALOG NUMBER - 523821 is an FDA 510(k)-cleared medical device (K914690) manufactured by Edward Weck, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 22, 1992. Regulation: 8.