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Negocios · 1/5/20261 min de lectura

Medical Devices; Exemptions From Premarket Notification: Certain Class II Devices; Request for Comments

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Resumen

The Food and Drug Administration (FDA) is announcing its intent to exempt from premarket notification requirements certain class II clinical toxicology test system devices. FDA is publishing this notice and requesting public comment in accordance with procedures established by the 21st Century Cures Act. This notice does not represent FDA's final determination with respect to the devices included in this document. FDA will review any comments submitted within the 60-day comment period and will further consider whether the exemption described in this notice should be modified prior to publication of its final determination in the Federal Register.

Idioma original de la fuente: Federal Register — Food and Drug AdministrationAbrir el comunicado original →