牙科单元型号：Mare
K号: K231845 · 2024-02-28
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决定日期2024-02-28
产品代码EIA
咨询委员会DE
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决定实质等同
器械摘要
Dental unit Model: Mare is the device name listed in this FDA 510(k) record. The listed applicant is Foshan Safety Medical Equipment Co., Ltd.. It received FDA 510(k) clearance on 2024-02-28 under 510(k) number K231845. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Dental unit Model: Mare?
Dental unit Model: Mare is a medical device that received FDA 510(k) clearance on 2024-02-28. The listed applicant is Foshan Safety Medical Equipment Co., Ltd.. The 510(k) number is K231845.
When did Dental unit Model: Mare receive FDA 510(k) clearance?
Dental unit Model: Mare received FDA 510(k) clearance on 2024-02-28, under 510(k) number K231845.
Who is the listed applicant for Dental unit Model: Mare?
The FDA 510(k) record lists Foshan Safety Medical Equipment Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Dental unit Model: Mare?
The FDA product code for Dental unit Model: Mare is EIA.
相关临床试验
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：EIA）
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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