Swift Ray 1
K号: K251678 · 2026-02-24
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决定日期2026-02-24
产品代码QJF
咨询委员会SU
请注意，您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同
器械摘要
Swift Ray 1 is the device name listed in this FDA 510(k) record. The listed applicant is Swift Medical, Inc.. It received FDA 510(k) clearance on 2026-02-24 under 510(k) number K251678. The device is classified under product code QJF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Swift Ray 1?
Swift Ray 1 is a medical device that received FDA 510(k) clearance on 2026-02-24. The listed applicant is Swift Medical, Inc.. The 510(k) number is K251678.
When did Swift Ray 1 receive FDA 510(k) clearance?
Swift Ray 1 received FDA 510(k) clearance on 2026-02-24, under 510(k) number K251678.
Who is the listed applicant for Swift Ray 1?
The FDA 510(k) record lists Swift Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Swift Ray 1?
The FDA product code for Swift Ray 1 is QJF.
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相关器械（代码：QJF）
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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