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Alpha-Omega Services, Inc.
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AOS UNIVERSAL CONECTING GUIDE TUBE is an FDA 510(k)-cleared medical device (K062824) manufactured by Alpha-Omega Services, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 2, 2007. Regulation: 8.