Curapuls 670
K号: K243112 · 2025-06-25
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决定日期2025-06-25
产品代码IMJ
咨询委员会PM
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器械摘要
Curapuls 670 is the device name listed in this FDA 510(k) record. The listed applicant is Enraf-Nonius, B.V.. It received FDA 510(k) clearance on 2025-06-25 under 510(k) number K243112. The device is classified under product code IMJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Curapuls 670?
Curapuls 670 is a medical device that received FDA 510(k) clearance on 2025-06-25. The listed applicant is Enraf-Nonius, B.V.. The 510(k) number is K243112.
When did Curapuls 670 receive FDA 510(k) clearance?
Curapuls 670 received FDA 510(k) clearance on 2025-06-25, under 510(k) number K243112.
Who is the listed applicant for Curapuls 670?
The FDA 510(k) record lists Enraf-Nonius, B.V. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Curapuls 670?
The FDA product code for Curapuls 670 is IMJ.
相关临床试验
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列明Enraf-Nonius, B.V.为申报人的其他记录
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。
相关器械（代码：IMJ）
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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