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Northeast Scientific, Inc.
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NES REPROCESSED VARICOSE VEIN RF CATHETER is an FDA 510(k)-cleared medical device (K090661) manufactured by Northeast Scientific, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 20, 2010. Regulation: 8.