G210 InviCell Plus with SignipHy pH 监测
K号: K191020 · 2020-01-14
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决定日期2020-01-14
产品代码PUB
咨询委员会OB
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决定实质等同
器械摘要
G210 InviCell Plus with SignipHy pH monitoring is the device name listed in this FDA 510(k) record. The listed applicant is CooperSurgical, Inc.. It received FDA 510(k) clearance on 2020-01-14 under 510(k) number K191020. The device is classified under product code PUB. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the G210 InviCell Plus with SignipHy pH monitoring?
G210 InviCell Plus with SignipHy pH monitoring is a medical device that received FDA 510(k) clearance on 2020-01-14. The listed applicant is CooperSurgical, Inc.. The 510(k) number is K191020.
When did G210 InviCell Plus with SignipHy pH monitoring receive FDA 510(k) clearance?
G210 InviCell Plus with SignipHy pH monitoring received FDA 510(k) clearance on 2020-01-14, under 510(k) number K191020.
Who is the listed applicant for G210 InviCell Plus with SignipHy pH monitoring?
FDA 510(k)记录中列出CooperSurgical, Inc.为申请人。这本身并不足以确立设备制造商。
What is the FDA product code for G210 InviCell Plus with SignipHy pH monitoring?
The FDA product code for G210 InviCell Plus with SignipHy pH monitoring is PUB.
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CooperSurgical, Inc.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。
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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