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Neurotherapies Reset GmbH

FDA 510(k) & PMA Approved Devices — 1 products

Total Devices1
Categories1
Latest FDA decision2016-01-20
TypeNumberDevice NameCodeDateActions
510(k) K151558 Desyncra for Tinnitus Therapy System, Desyncra for Tinnitus Pro SystemKLW2016-01-20 View