Spectral CT 7500 RT
K号: K240844 · 2024-10-18
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器械摘要
Spectral CT 7500 RT is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems Technologies , Ltd.. It received FDA 510(k) clearance on 2024-10-18 under 510(k) number K240844. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Spectral CT 7500 RT?
Spectral CT 7500 RT is a medical device that received FDA 510(k) clearance on 2024-10-18. The listed applicant is Philips Medical Systems Technologies , Ltd.. The 510(k) number is K240844.
When did Spectral CT 7500 RT receive FDA 510(k) clearance?
Spectral CT 7500 RT received FDA 510(k) clearance on 2024-10-18, under 510(k) number K240844.
Who is the listed applicant for Spectral CT 7500 RT?
The FDA 510(k) record lists Philips Medical Systems Technologies , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Spectral CT 7500 RT?
The FDA product code for Spectral CT 7500 RT is JAK.
相关临床试验
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列明Philips Medical Systems Technologies , Ltd.为申报人的其他记录
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：JAK）
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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