Fed Regist. 1985 Oct 23;50(205):43060-81.
The Food and Drug Administration (FDA) is announcing its policy for setting priorities for initiating proceedings to establish performance standards for medical devices classified into class II, a category of devices under the Medical Device Amendments for which FDA is required to establish performance standards. At this time, however, FDA does not have the resources to establish performance standards for all class II devices. Accordingly, the policy describes the factors the agency takes into account in establishing priorities for initiating standard-setting proceedings.
美国食品药品监督管理局(FDA)正在宣布其关于确定启动程序优先级的政策,该程序旨在为被归类为II类的医疗器械制定性能标准,II类医疗器械是《医疗器械修正案》规定的一类器械,FDA必须为其制定性能标准。然而,目前FDA没有资源为所有II类器械制定性能标准。因此,该政策描述了该机构在确定启动标准制定程序的优先级时所考虑的因素。