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Zdrowie i gospodarka · 24/10/2006

FDA Announces Exemptions for Cranial Orthosis Type Devices

The FDA is seeking public comments on a petition to exempt cranial orthosis type devices, used to improve cranial symmetry in newborns, from premarket notification requirements, as mandated by the Food and Drug Administration Modernization Act of 1997.

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