离子-L
K号: K261209 · 2026-06-11
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器械摘要
Ion-L is the device name listed in this FDA 510(k) record. The listed applicant is SurGenTec, LLC. It received FDA 510(k) clearance on 2026-06-11 under 510(k) number K261209. The device is classified under product code MRW. FDA Decision: Substantially Equivalent.
常见问题
What is the Ion-L?
Ion-L is a medical device that received FDA 510(k) clearance on 2026-06-11. The listed applicant is SurGenTec, LLC. The 510(k) number is K261209.
When did Ion-L receive FDA 510(k) clearance?
Ion-L received FDA 510(k) clearance on 2026-06-11, under 510(k) number K261209.
Who is the listed applicant for Ion-L?
FDA 510(k)记录中列出SurGenTec, LLC为申请人。这本身并不能确立该设备的制造商。
What is the FDA product code for Ion-L?
The FDA product code for Ion-L is MRW.
列明SurGenTec, LLC为申报人的其他记录
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：MRW）
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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