数字彩色多普勒超声系统(P60系列)
K号: K241949 · 2025-01-17
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器械摘要
常见问题
What is the Digital Color Doppler Ultrasound System (P60 Series)?
Digital Color Doppler Ultrasound System (P60 Series) is a medical device that received FDA 510(k) clearance on 2025-01-17. The listed applicant is Sonoscape Medical Corp.. The 510(k) number is K241949.
When did Digital Color Doppler Ultrasound System (P60 Series) receive FDA 510(k) clearance?
Digital Color Doppler Ultrasound System (P60 Series) received FDA 510(k) clearance on 2025-01-17, under 510(k) number K241949.
Who is the listed applicant for Digital Color Doppler Ultrasound System (P60 Series)?
FDA 510(k)记录将Sonoscape Medical Corp.列为申请人。这本身并不能确立该设备制造商的身份。
What is the FDA product code for Digital Color Doppler Ultrasound System (P60 Series)?
The FDA product code for Digital Color Doppler Ultrasound System (P60 Series) is IYN.
相关临床试验
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。
列明Sonoscape Medical Corp.为申报人的其他记录
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。
相关器械(代码:IYN)
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息,请务必参考官方记录。
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