DOOPANG
K号: K232749 · 2024-06-11
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申请人Ybrain, Inc.
决定日期2024-06-11
产品代码PCC
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
DOOPANG is the device name listed in this FDA 510(k) record. The listed applicant is Ybrain, Inc.. It received FDA 510(k) clearance on 2024-06-11 under 510(k) number K232749. The device is classified under product code PCC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the DOOPANG?
DOOPANG is a medical device that received FDA 510(k) clearance on 2024-06-11. The listed applicant is Ybrain, Inc.. The 510(k) number is K232749.
When did DOOPANG receive FDA 510(k) clearance?
DOOPANG received FDA 510(k) clearance on 2024-06-11, under 510(k) number K232749.
Who is the listed applicant for DOOPANG?
The FDA 510(k) record lists Ybrain, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DOOPANG?
The FDA product code for DOOPANG is PCC.
相关临床试验
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相关器械（代码：PCC）
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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