Heat Pain Pro
K号: K181992 · 2018-11-09
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决定日期2018-11-09
产品代码NUH
咨询委员会NE
请注意，您提供的文本“NE”不足以进行翻译，因为它不是一个完整的句子或描述。请提供完整的医疗设备监管文本，以便我能够进行准确的翻译。
决定实质等同
器械摘要
Heat Pain Pro is the device name listed in this FDA 510(k) record. The listed applicant is Omron Healthcare, Inc.. It received FDA 510(k) clearance on 2018-11-09 under 510(k) number K181992. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Heat Pain Pro?
Heat Pain Pro is a medical device that received FDA 510(k) clearance on 2018-11-09. The listed applicant is Omron Healthcare, Inc.. The 510(k) number is K181992.
When did Heat Pain Pro receive FDA 510(k) clearance?
Heat Pain Pro received FDA 510(k) clearance on 2018-11-09, under 510(k) number K181992.
Who is the listed applicant for Heat Pain Pro?
The FDA 510(k) record lists Omron Healthcare, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Heat Pain Pro?
The FDA product code for Heat Pain Pro is NUH.
列明Omron Healthcare, 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。
相关器械（代码：NUH）
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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