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Avalon Laboratories, LLC
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AVALON ELITE MULTI-PORT VENOUS FEMORAL CATHETER, 20FR, 22FR, 24FR, 26FR, 28FR is an FDA 510(k)-cleared medical device (K081933) manufactured by Avalon Laboratories, LLC. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 2, 2008. Regulation: 8.