
Silq Technologies Corporation
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2-Way 100% Silicone ClearTract Catheter is an FDA 510(k)-cleared medical device (K221625) manufactured by Silq Technologies Corporation. 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 June 30, 2022. Regulation: 8.