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Zdrowie i gospodarka · 08/02/1999

FDA Proposes Reclassification of Extracorporeal Shock Wave Lithotripter

The FDA is seeking public comment on a proposal to reclassify the extracorporeal shock wave lithotripter from Class III to Class II for use in treating kidney and ureteral stones, following a recommendation from the Gastroenterology and Urology Devices Advisory Panel.

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