
Acumed Medical Supplies , Ltd.
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TENS PRO 900 is an FDA 510(k)-cleared medical device (K023726) manufactured by Acumed Medical Supplies , Ltd.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 16, 2003. Regulation: 8.