Philips CT Big Bore
K号: K171850 · 2017-11-09
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器械摘要
Philips CT Big Bore is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems (Cleveland), Inc.. It received FDA 510(k) clearance on 2017-11-09 under 510(k) number K171850. 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 CT Big Bore?
Philips CT Big Bore is a medical device that received FDA 510(k) clearance on 2017-11-09. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K171850.
When did Philips CT Big Bore receive FDA 510(k) clearance?
Philips CT Big Bore received FDA 510(k) clearance on 2017-11-09, under 510(k) number K171850.
Who is the listed applicant for Philips CT Big Bore?
The FDA 510(k) record lists Philips Medical Systems (Cleveland), Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Philips CT Big Bore?
The FDA product code for Philips CT Big Bore is JAK.
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列明Philips Medical Systems (Cleveland), Inc.为申报人的其他记录
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相关器械（代码：JAK）
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官方来源
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