PRO-DOSE系统
K号: K250083 · 2025-10-01
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器械摘要
PRO-DOSE System is the device name listed in this FDA 510(k) record. The listed applicant is Nu-Rise, SA. It received FDA 510(k) clearance on 2025-10-01 under 510(k) number K250083. The device is classified under product code NZT. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the PRO-DOSE System?
PRO-DOSE System is a medical device that received FDA 510(k) clearance on 2025-10-01. The listed applicant is Nu-Rise, SA. The 510(k) number is K250083.
When did PRO-DOSE System receive FDA 510(k) clearance?
PRO-DOSE System received FDA 510(k) clearance on 2025-10-01, under 510(k) number K250083.
Who is the listed applicant for PRO-DOSE System?
The FDA 510(k) record lists Nu-Rise, SA as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PRO-DOSE System?
The FDA product code for PRO-DOSE System is NZT.
相关临床试验
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相关器械（代码：NZT）
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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