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Zdrowie i gospodarka · 15/11/2013

FDA Classifies Scleral Plug into Class II, Exempts Certain Devices from 510(k) Requirements

The FDA has classified the scleral plug into class II, exempting devices made from surgical grade stainless steel from premarket notification requirements, while still requiring premarket notification for other devices, to ensure safety and effectiveness.

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