
Sonowand AS
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GENERAL PRUPOSE LOCALIZERS AND ADAPTERS-NEW ACCESSORIES FOR SONOWAND SYSTEM is an FDA 510(k)-cleared medical device (K112469) manufactured by Sonowand AS. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 22, 2012. Regulation: 8.