Deltaven XiV Max, Deltaven XiV Max FF
K号: K171530 · 2017-12-21
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决定日期2017-12-21
产品代码FOZ
咨询委员会医疗设备监管文本翻译如下：
HO
请注意，由于您没有提供具体的医疗设备监管文本内容，以上仅为示例。请提供具体的文本内容以便进行准确的翻译。
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器械摘要
Deltaven XiV Max, Deltaven XiV Max FF is the device name listed in this FDA 510(k) record. The listed applicant is Delta Med Spa. It received FDA 510(k) clearance on 2017-12-21 under 510(k) number K171530. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Deltaven XiV Max, Deltaven XiV Max FF?
Deltaven XiV Max, Deltaven XiV Max FF is a medical device that received FDA 510(k) clearance on 2017-12-21. The listed applicant is Delta Med Spa. The 510(k) number is K171530.
When did Deltaven XiV Max, Deltaven XiV Max FF receive FDA 510(k) clearance?
Deltaven XiV Max, Deltaven XiV Max FF received FDA 510(k) clearance on 2017-12-21, under 510(k) number K171530.
Who is the listed applicant for Deltaven XiV Max, Deltaven XiV Max FF?
The FDA 510(k) record lists Delta Med Spa as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Deltaven XiV Max, Deltaven XiV Max FF?
The FDA product code for Deltaven XiV Max, Deltaven XiV Max FF is FOZ.
相关临床试验
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列明Delta Med Spa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：FOZ）
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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