
Travenol Laboratories, S.A.
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SOLUTION ADMINI. SETS- ALTER. DRIP CHAMBER/CONNEC. is an FDA 510(k)-cleared medical device (K870940) manufactured by Travenol Laboratories, S.A.. 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 March 16, 1987. Regulation: 8.

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