Airdog X8空气净化器（KJ800F-X8）
K号: K240696 · 2024-06-14
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决定日期2024-06-14
产品代码FRF
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。
决定实质等同
器械摘要
Airdog X8 Air Purifier (KJ800F-X8) is the device name listed in this FDA 510(k) record. The listed applicant is Suzhou Beiang Smart Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-06-14 under 510(k) number K240696. The device is classified under product code FRF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Airdog X8 Air Purifier (KJ800F-X8)?
Airdog X8 Air Purifier (KJ800F-X8) is a medical device that received FDA 510(k) clearance on 2024-06-14. The listed applicant is Suzhou Beiang Smart Technology Co., Ltd.. The 510(k) number is K240696.
When did Airdog X8 Air Purifier (KJ800F-X8) receive FDA 510(k) clearance?
Airdog X8 Air Purifier (KJ800F-X8) received FDA 510(k) clearance on 2024-06-14, under 510(k) number K240696.
Who is the listed applicant for Airdog X8 Air Purifier (KJ800F-X8)?
The FDA 510(k) record lists Suzhou Beiang Smart Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Airdog X8 Air Purifier (KJ800F-X8)?
The FDA product code for Airdog X8 Air Purifier (KJ800F-X8) is FRF.
相关临床试验
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相关器械（代码：FRF）
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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