
Travenol Laboratories, S.A.
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CF/211 CAPILLARY FLOW DIALYZER, #5M1784 is an FDA 510(k)-cleared medical device (K800221) 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 February 25, 1980. Regulation: 8.