Varios Combi Pro2
K号: K260773 · 2026-03-10
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决定日期2026-03-10
产品代码ELC
咨询委员会DE
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决定实质等同
器械摘要
Varios Combi Pro2 is the device name listed in this FDA 510(k) record. The listed applicant is Nakanishi, Inc.. It received FDA 510(k) clearance on 2026-03-10 under 510(k) number K260773. The device is classified under product code ELC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Varios Combi Pro2?
Varios Combi Pro2 is a medical device that received FDA 510(k) clearance on 2026-03-10. The listed applicant is Nakanishi, Inc.. The 510(k) number is K260773.
When did Varios Combi Pro2 receive FDA 510(k) clearance?
Varios Combi Pro2 received FDA 510(k) clearance on 2026-03-10, under 510(k) number K260773.
Who is the listed applicant for Varios Combi Pro2?
The FDA 510(k) record lists Nakanishi, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Varios Combi Pro2?
The FDA product code for Varios Combi Pro2 is ELC.
相关临床试验
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列明Nakanishi, Inc.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：ELC）
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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