PreOp v3
K号: K252565 · 2026-02-13
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决定日期2026-02-13
产品代码OLX
咨询委员会NE
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器械摘要
PreOp v3 is the device name listed in this FDA 510(k) record. The listed applicant is Clouds of Care. It received FDA 510(k) clearance on 2026-02-13 under 510(k) number K252565. The device is classified under product code OLX. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the PreOp v3?
PreOp v3 is a medical device that received FDA 510(k) clearance on 2026-02-13. The listed applicant is Clouds of Care. The 510(k) number is K252565.
When did PreOp v3 receive FDA 510(k) clearance?
PreOp v3 received FDA 510(k) clearance on 2026-02-13, under 510(k) number K252565.
Who is the listed applicant for PreOp v3?
The FDA 510(k) record lists Clouds of Care as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PreOp v3?
The FDA product code for PreOp v3 is OLX.
相关临床试验
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相关器械（代码：OLX）
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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