Maxtec MaxO2 ME+p
K号: K221734 · 2023-04-01
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申请人Maxtec, LLC
决定日期2023-04-01
产品代码CCL
咨询委员会AN
请注意，由于您没有提供完整的医疗设备监管文本，我无法提供完整的翻译。如果您能提供完整的文本，我将很乐意为您翻译。
决定实质等同
器械摘要
Maxtec MaxO2 ME+p is the device name listed in this FDA 510(k) record. The listed applicant is Maxtec, LLC. It received FDA 510(k) clearance on 2023-04-01 under 510(k) number K221734. The device is classified under product code CCL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Maxtec MaxO2 ME+p?
Maxtec MaxO2 ME+p is a medical device that received FDA 510(k) clearance on 2023-04-01. The listed applicant is Maxtec, LLC. The 510(k) number is K221734.
When did Maxtec MaxO2 ME+p receive FDA 510(k) clearance?
Maxtec MaxO2 ME+p received FDA 510(k) clearance on 2023-04-01, under 510(k) number K221734.
Who is the listed applicant for Maxtec MaxO2 ME+p?
The FDA 510(k) record lists Maxtec, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Maxtec MaxO2 ME+p?
The FDA product code for Maxtec MaxO2 ME+p is CCL.
相关临床试验
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列明Maxtec, LLC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：CCL）
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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