VELO 呼吸测试
K号: K251742 · 2026-02-13
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决定日期2026-02-13
产品代码QOF
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器械摘要
VELO Respiratory Test is the device name listed in this FDA 510(k) record. The listed applicant is Lex Diagnostics Limited. It received FDA 510(k) clearance on 2026-02-13 under 510(k) number K251742. The device is classified under product code QOF. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the VELO Respiratory Test?
VELO Respiratory Test is a medical device that received FDA 510(k) clearance on 2026-02-13. The listed applicant is Lex Diagnostics Limited. The 510(k) number is K251742.
When did VELO Respiratory Test receive FDA 510(k) clearance?
VELO Respiratory Test received FDA 510(k) clearance on 2026-02-13, under 510(k) number K251742.
Who is the listed applicant for VELO Respiratory Test?
The FDA 510(k) record lists Lex Diagnostics Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VELO Respiratory Test?
The FDA product code for VELO Respiratory Test is QOF.
相关临床试验
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相关器械（代码：QOF）
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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