Philips Incisive CT拖车
K号: K211168 · 2021-11-22
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器械摘要
Philips Incisive CT on Trailer is the device name listed in this FDA 510(k) record. The listed applicant is Philips Healthcare (Suzhou) Co., Ltd.. It received FDA 510(k) clearance on 2021-11-22 under 510(k) number K211168. 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 Philips Incisive CT on Trailer?
Philips Incisive CT on Trailer is a medical device that received FDA 510(k) clearance on 2021-11-22. The listed applicant is Philips Healthcare (Suzhou) Co., Ltd.. The 510(k) number is K211168.
When did Philips Incisive CT on Trailer receive FDA 510(k) clearance?
Philips Incisive CT on Trailer received FDA 510(k) clearance on 2021-11-22, under 510(k) number K211168.
Who is the listed applicant for Philips Incisive CT on Trailer?
The FDA 510(k) record lists Philips Healthcare (Suzhou) Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Philips Incisive CT on Trailer?
The FDA product code for Philips Incisive CT on Trailer is JAK.
相关临床试验
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列明Philips Healthcare (Suzhou) Co., 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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