K261412
- 510(k) 号
- K261412
- 器械名称
- V8/XV8/XH8/H8/cV8/V8 ONE/XV8 ONE/XH8 ONE/H8 ONE/cV8 ONE Diagnostic Ultrasound System; V7/XV7/XH7/H7/cV7/V7 ONE/XV7 ONE/H7 ONE/XH7 ONE/cV7 ONE Diagnostic Ultrasound System; V6/XV6/XH6/H6/cV6/V6 ONE/XV6 ONE/H6 ONE/XH6 ONE/cV6 ONE Diagnostic Ultrasound System; V5/XV5/XH5/H5/cV5 Diagnostic Ultrasound System; V4/XV4/XH4/H4/cV4 Diagnostic Ultrasound System;
- 申请人
- Samsung Medison Co., Ltd. KR
- 产品代码
- IYN — System, Imaging, Pulsed Doppler, Ultrasonic
- 批准日期
- 2026-07-28
- 受理日期
- 2026-04-30
- 决定
- Substantially Equivalent
- 审查途径
- Traditional
- 咨询委员会
- Radiology
FDA 官方记录: K261412
数据来自 openFDA 510(k) 数据集(CC0 公有领域),以 FDA 现行记录为准。510(k) 许可不等于 FDA 认证或批准。