Eagle S/Saevo Slim/D700 Slim
K号: K230732 · 2023-04-11
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决定日期2023-04-11
产品代码MUH
咨询委员会DE
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决定实质等同
器械摘要
Eagle S/Saevo Slim/D700 Slim is the device name listed in this FDA 510(k) record. The listed applicant is Alliage S/A Industrias Medica Odontológico.. It received FDA 510(k) clearance on 2023-04-11 under 510(k) number K230732. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Eagle S/Saevo Slim/D700 Slim?
Eagle S/Saevo Slim/D700 Slim is a medical device that received FDA 510(k) clearance on 2023-04-11. The listed applicant is Alliage S/A Industrias Medica Odontológico.. The 510(k) number is K230732.
When did Eagle S/Saevo Slim/D700 Slim receive FDA 510(k) clearance?
Eagle S/Saevo Slim/D700 Slim received FDA 510(k) clearance on 2023-04-11, under 510(k) number K230732.
Who is the listed applicant for Eagle S/Saevo Slim/D700 Slim?
The FDA 510(k) record lists Alliage S/A Industrias Medica Odontológico. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Eagle S/Saevo Slim/D700 Slim?
The FDA product code for Eagle S/Saevo Slim/D700 Slim is MUH.
相关临床试验
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相关器械（代码：MUH）
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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