E5 Series Digital Color Doppler Ultrasound System
K号: K170303 · 2017-05-19
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器械摘要
E5 Series Digital Color Doppler Ultrasound System is the device name listed in this FDA 510(k) record. The listed applicant is Sonoscape Medical Corp.. It received FDA 510(k) clearance on 2017-05-19 under 510(k) number K170303. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the E5 Series Digital Color Doppler Ultrasound System?
E5 Series Digital Color Doppler Ultrasound System is a medical device that received FDA 510(k) clearance on 2017-05-19. The listed applicant is Sonoscape Medical Corp.. The 510(k) number is K170303.
When did E5 Series Digital Color Doppler Ultrasound System receive FDA 510(k) clearance?
E5 Series Digital Color Doppler Ultrasound System received FDA 510(k) clearance on 2017-05-19, under 510(k) number K170303.
Who is the listed applicant for E5 Series Digital Color Doppler Ultrasound System?
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 E5 Series Digital Color Doppler Ultrasound System?
The FDA product code for E5 Series Digital Color Doppler Ultrasound System is IYN.
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列明Sonoscape Medical Corp.为申报人的其他记录
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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。
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官方来源
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