OKI

Emergency Response Safety Kit

产品代码
OKI
器械名称
Emergency Response Safety Kit
管理类别
第 2 类(Class II)
21 CFR 条款
21 CFR 878.4040
FDA 专业组
General, Plastic Surgery
上市路径
Enforcement Discretion

FDA 分类定义

This product code has been established in accordance with the May 20, 1997, Guidance entitled, Convenience Kits Interim Regulatory Guidance, found at www.fda.gov/cdrh/ode/convkit.html. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.

定义原文来自 FDA 器械分类库,属美国联邦政府作品(公有领域)。

FDA 官方分类页: OKI
分类与上市路径以 FDA 现行公告为准。本页数据来自 openFDA(CC0 公有领域),不构成注册策略建议。