BiliWrap
K号: K243372 · 2025-05-29
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决定日期2025-05-29
产品代码LBI
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
BiliWrap is the device name listed in this FDA 510(k) record. The listed applicant is Gerium Medical, Ltd.. It received FDA 510(k) clearance on 2025-05-29 under 510(k) number K243372. The device is classified under product code LBI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the BiliWrap?
BiliWrap is a medical device that received FDA 510(k) clearance on 2025-05-29. The listed applicant is Gerium Medical, Ltd.. The 510(k) number is K243372.
When did BiliWrap receive FDA 510(k) clearance?
BiliWrap received FDA 510(k) clearance on 2025-05-29, under 510(k) number K243372.
Who is the listed applicant for BiliWrap?
The FDA 510(k) record lists Gerium Medical, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BiliWrap?
The FDA product code for BiliWrap is LBI.
相关临床试验
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相关器械（代码：LBI）
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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