Jason 膜
K号: K242817 · 2025-12-12
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决定日期2025-12-12
产品代码NPL
咨询委员会DE
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决定实质等同
器械摘要
Jason membrane is the device name listed in this FDA 510(k) record. The listed applicant is Botiss Biomaterials GmbH. It received FDA 510(k) clearance on 2025-12-12 under 510(k) number K242817. The device is classified under product code NPL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Jason membrane?
Jason membrane is a medical device that received FDA 510(k) clearance on 2025-12-12. The listed applicant is Botiss Biomaterials GmbH. The 510(k) number is K242817.
When did Jason membrane receive FDA 510(k) clearance?
Jason membrane received FDA 510(k) clearance on 2025-12-12, under 510(k) number K242817.
Who is the listed applicant for Jason membrane?
The FDA 510(k) record lists Botiss Biomaterials GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Jason membrane?
The FDA product code for Jason membrane is NPL.
相关临床试验
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相关器械（代码：NPL）
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
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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