
Teva Medical, Ltd.
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FREE FLOW SAFETY DEVICE, MODEL MG 245052 is an FDA 510(k)-cleared medical device (K990288) manufactured by Teva Medical, Ltd.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 23, 1999. Regulation: 8.

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