CS-Pro MED
K号: K250779 · 2025-07-02
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决定日期2025-07-02
产品代码PZL
咨询委员会SU
请注意，您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同
器械摘要
CS-Pro MED is the device name listed in this FDA 510(k) record. The listed applicant is Curative Sound Therapeutics. It received FDA 510(k) clearance on 2025-07-02 under 510(k) number K250779. The device is classified under product code PZL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the CS-Pro MED?
CS-Pro MED is a medical device that received FDA 510(k) clearance on 2025-07-02. The listed applicant is Curative Sound Therapeutics. The 510(k) number is K250779.
When did CS-Pro MED receive FDA 510(k) clearance?
CS-Pro MED received FDA 510(k) clearance on 2025-07-02, under 510(k) number K250779.
Who is the listed applicant for CS-Pro MED?
The FDA 510(k) record lists Curative Sound Therapeutics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CS-Pro MED?
The FDA product code for CS-Pro MED is PZL.
相关器械（代码：PZL）
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
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