medXion NEXUS
K号: K253935 · 2026-05-15
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器械摘要
medXion NEXUS is the device name listed in this FDA 510(k) record. The listed applicant is medXion Technologies, Inc.. It received FDA 510(k) clearance on 2026-05-15 under 510(k) number K253935. The device is classified under product code OAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the medXion NEXUS?
medXion NEXUS is a medical device that received FDA 510(k) clearance on 2026-05-15. The listed applicant is medXion Technologies, Inc.. The 510(k) number is K253935.
When did medXion NEXUS receive FDA 510(k) clearance?
medXion NEXUS received FDA 510(k) clearance on 2026-05-15, under 510(k) number K253935.
Who is the listed applicant for medXion NEXUS?
The FDA 510(k) record lists medXion Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for medXion NEXUS?
The FDA product code for medXion NEXUS is OAS.
相关临床试验
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相关器械（代码：OAS）
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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