
Rhythmlink International, LLC
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RHYTHMLINK DISPOSABLE MONOPOLAR EMG NEEDLE, MODEL TFDN26032252R is an FDA 510(k)-cleared medical device (K091056) manufactured by Rhythmlink International, LLC. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 22, 2009. Regulation: 8.