Breathe+
K号: K222018 · 2023-06-02
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决定日期2023-06-02
产品代码BWF
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
Breathe+ is the device name listed in this FDA 510(k) record. The listed applicant is Peep Medical, LLC Dba Go2 Devices. It received FDA 510(k) clearance on 2023-06-02 under 510(k) number K222018. The device is classified under product code BWF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Breathe+?
Breathe+ is a medical device that received FDA 510(k) clearance on 2023-06-02. The listed applicant is Peep Medical, LLC Dba Go2 Devices. The 510(k) number is K222018.
When did Breathe+ receive FDA 510(k) clearance?
Breathe+ received FDA 510(k) clearance on 2023-06-02, under 510(k) number K222018.
Who is the listed applicant for Breathe+?
The FDA 510(k) record lists Peep Medical, LLC Dba Go2 Devices as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Breathe+?
The FDA product code for Breathe+ is BWF.
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：BWF）
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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