
Travenol Laboratories, S.A.
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CAPILLARY FLOW DIALYZERS is an FDA 510(k)-cleared medical device (K870169) manufactured by Travenol Laboratories, S.A.. 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 April 5, 1987. Regulation: 8.