
Nihon Kohden Corp.
Free shipping on orders over $99 · 30-day returns
PE-210AK SWITCH BOX is an FDA 510(k)-cleared medical device (K110376) manufactured by Nihon Kohden Corp.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 28, 2011. Regulation: 8.