DigitalDiagnost C50
K号: K201725 · 2020-07-10
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器械摘要
DigitalDiagnost C50 is the device name listed in this FDA 510(k) record. The listed applicant is Philips Healthcare (Suzhou) Co., Lit.. It received FDA 510(k) clearance on 2020-07-10 under 510(k) number K201725. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the DigitalDiagnost C50?
DigitalDiagnost C50 is a medical device that received FDA 510(k) clearance on 2020-07-10. The listed applicant is Philips Healthcare (Suzhou) Co., Lit.. The 510(k) number is K201725.
When did DigitalDiagnost C50 receive FDA 510(k) clearance?
DigitalDiagnost C50 received FDA 510(k) clearance on 2020-07-10, under 510(k) number K201725.
Who is the listed applicant for DigitalDiagnost C50?
The FDA 510(k) record lists Philips Healthcare (Suzhou) Co., Lit. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DigitalDiagnost C50?
The FDA product code for DigitalDiagnost C50 is KPR.
相关临床试验
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：KPR）
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
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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