ONG
- 产品代码
- ONG
- 器械名称
- Powered Laser Surgical Instrument With MicrobeamFractional Output
- 管理类别
- 第 2 类(Class II)
- 21 CFR 条款
- 21 CFR 878.4810
- FDA 专业组
- General, Plastic Surgery
- 上市路径
- 需提交 510(k) 上市前通告
- 标记
- 可走第三方审查
- 该代码近三年的 510(k)
- 5 件
- 其中 Summary 已存档
- 4 份,可直接下载
- FDA 历史累计 510(k)
- 35 件(全部年份;本站只收录近三年的明细)
FDA 分类定义
A LASER (Light Amplification by Stimulated Emission of Radiation) based device having coherence, collimated and typically monochromatic radiation. The laser output is in form of tiny beams in micro range. Typically, indicated to be used in medical specialties of general and plastic surgery and of dermatology/aesthetic to destroy, remove or coagulate tissue, generally soft tissue. Indication for Use can be general and/or specific. The classification regulation 21 CFR 878.4810 describes a device that is carbon dioxide or argon laser intended to cut, destroy, remove or coagulate tissue by the light.
该代码近三年的 510(k)(5 件)
| 510(k) 号 | 批准日期 | 申请人 | 器械名称 | 摘要 |
|---|---|---|---|---|
| K252155 | 2025-10-20 | AVAVA, Inc. | AVAVA Skin Treatment System | |
| K244060 | 2025-07-31 | Lutronic Corporation | eCO2 3D | |
| K251031 | 2025-07-02 | Shanghai Apolo Medical Technology Co.,… | Fiber Laser Treatment Systems (HS-232,HS-233) | |
| K250402 | 2025-04-14 | AVAVA, Inc. | AVAVA Skin Treatment System | FDA |
| K233550 | 2024-01-02 | Lutronic Aesthetic | MOSAIC 3D (Surgical Laser) |
FDA 官方分类页: ONG
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。