空气压缩按摩器（ACM-PLUS-A1，ACM-PLUS-A2，ACM-PLUS-A3，ACM-PLUS-A4，ACM-PLUS-A5，ACM-PLUS-A6）
K号: K243206 · 2025-02-19
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器械摘要
常见问题
What is the Air compression massager (ACM-PLUS-A1, ACM-PLUS-A2, ACM-PLUS-A3, ACM-PLUS-A4, ACM-PLUS-A5, ACM-PLUS-A6)?
Air compression massager (ACM-PLUS-A1, ACM-PLUS-A2, ACM-PLUS-A3, ACM-PLUS-A4, ACM-PLUS-A5, ACM-PLUS-A6) is a medical device that received FDA 510(k) clearance on 2025-02-19. The listed applicant is Sichuan Qianli-Beoka Medical Technology, Inc.. The 510(k) number is K243206.
When did Air compression massager (ACM-PLUS-A1, ACM-PLUS-A2, ACM-PLUS-A3, ACM-PLUS-A4, ACM-PLUS-A5, ACM-PLUS-A6) receive FDA 510(k) clearance?
Air compression massager (ACM-PLUS-A1, ACM-PLUS-A2, ACM-PLUS-A3, ACM-PLUS-A4, ACM-PLUS-A5, ACM-PLUS-A6) received FDA 510(k) clearance on 2025-02-19, under 510(k) number K243206.
Who is the listed applicant for Air compression massager (ACM-PLUS-A1, ACM-PLUS-A2, ACM-PLUS-A3, ACM-PLUS-A4, ACM-PLUS-A5, ACM-PLUS-A6)?
The FDA 510(k) record lists Sichuan Qianli-Beoka Medical Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Air compression massager (ACM-PLUS-A1, ACM-PLUS-A2, ACM-PLUS-A3, ACM-PLUS-A4, ACM-PLUS-A5, ACM-PLUS-A6)?
The FDA product code for Air compression massager (ACM-PLUS-A1, ACM-PLUS-A2, ACM-PLUS-A3, ACM-PLUS-A4, ACM-PLUS-A5, ACM-PLUS-A6) is IRP.
相关临床试验
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相关器械（代码：IRP）
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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