OKLand 患者返回电极垫
K号: K183148 · 2020-02-04
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决定日期2020-02-04
产品代码GEI
咨询委员会SU
请注意，您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同
器械摘要
OKLand Patient Return Electrode Pad is the device name listed in this FDA 510(k) record. The listed applicant is Auckland Medical Polymer(Tianjin) Co., Ltd.. It received FDA 510(k) clearance on 2020-02-04 under 510(k) number K183148. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the OKLand Patient Return Electrode Pad?
OKLand Patient Return Electrode Pad is a medical device that received FDA 510(k) clearance on 2020-02-04. The listed applicant is Auckland Medical Polymer(Tianjin) Co., Ltd.. The 510(k) number is K183148.
When did OKLand Patient Return Electrode Pad receive FDA 510(k) clearance?
OKLand Patient Return Electrode Pad received FDA 510(k) clearance on 2020-02-04, under 510(k) number K183148.
Who is the listed applicant for OKLand Patient Return Electrode Pad?
The FDA 510(k) record lists Auckland Medical Polymer(Tianjin) Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OKLand Patient Return Electrode Pad?
The FDA product code for OKLand Patient Return Electrode Pad is GEI.
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。
相关器械（代码：GEI）
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
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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