一次性预防性角度
K号: K240950 · 2025-05-28
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决定日期2025-05-28
产品代码EGS
咨询委员会DE
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器械摘要
Disposable Prophy Angle is the device name listed in this FDA 510(k) record. The listed applicant is Pacific Care Limited. It received FDA 510(k) clearance on 2025-05-28 under 510(k) number K240950. The device is classified under product code EGS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Disposable Prophy Angle?
Disposable Prophy Angle is a medical device that received FDA 510(k) clearance on 2025-05-28. The listed applicant is Pacific Care Limited. The 510(k) number is K240950.
When did Disposable Prophy Angle receive FDA 510(k) clearance?
Disposable Prophy Angle received FDA 510(k) clearance on 2025-05-28, under 510(k) number K240950.
Who is the listed applicant for Disposable Prophy Angle?
The FDA 510(k) record lists Pacific Care Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Disposable Prophy Angle?
The FDA product code for Disposable Prophy Angle is EGS.
相关临床试验
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相关器械（代码：EGS）
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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