一次性内用避孕套
PMA编号：P080002 · 2017-06-23
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决定日期2017-06-23
PMA 编号P080002
产品代码MBU
设备分类第2类
医疗专科O
法规编号21 CFR 8
咨询委员会OB
请注意，由于您没有提供具体的医疗设备监管文本，我无法进行翻译。请提供具体的文本内容，以便我能够按照您的要求进行翻译。
器械摘要
Single-use internal condom is the device name listed in this FDA 510(k) record. The listed applicant is Clear Future, Inc.. It received FDA 510(k) clearance on 2017-06-23. The device is classified under product code MBU. It was reviewed by the OB advisory panel.
常见问题
What is the Single-use internal condom?
Single-use internal condom is a medical device that received FDA 510(k) clearance on 2017-06-23. The listed applicant is Clear Future, Inc..
When did Single-use internal condom receive FDA 510(k) clearance?
The clearance date for Single-use internal condom can be found in the official FDA records.
Who is the listed applicant for Single-use internal condom?
The FDA 510(k) record lists Clear Future, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Single-use internal condom?
The FDA product code for Single-use internal condom is MBU.
相关临床试验
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相关 PubMed 文献
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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