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Usa Instruments, Inc.
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GEMINI III HYBRID TX/RX 4 CHANNEL HEAD COIL is an FDA 510(k)-cleared medical device (K033235) manufactured by Usa Instruments, 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 December 16, 2003. Regulation: 8.