
Unimed Surgical Products, Inc.
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NEEDLE ELCTRODE is an FDA 510(k)-cleared medical device (K944265) manufactured by Unimed Surgical Products, 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 May 4, 1995. Regulation: 8.