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Zdrowie i gospodarka · 20/02/2014

FDA Proposes Changes to Shortwave Diathermy Device Classification and Name

The Food and Drug Administration (FDA) is proposing to reclassify the shortwave diathermy device for non-medical uses from Class III to Class II, and rename it 'nonthermal shortwave therapy', based on new information and a technical correction to the regulation.

Source: Federal Register — Food and Drug AdministrationOpen original release →