PerfusionGo Plus
K号: K221627 · 2023-01-19
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器械摘要
PerfusionGo Plus is the device name listed in this FDA 510(k) record. The listed applicant is Yukun (Beijing) Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-01-19 under 510(k) number K221627. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the PerfusionGo Plus?
PerfusionGo Plus is a medical device that received FDA 510(k) clearance on 2023-01-19. The listed applicant is Yukun (Beijing) Technology Co., Ltd.. The 510(k) number is K221627.
When did PerfusionGo Plus receive FDA 510(k) clearance?
PerfusionGo Plus received FDA 510(k) clearance on 2023-01-19, under 510(k) number K221627.
Who is the listed applicant for PerfusionGo Plus?
The FDA 510(k) record lists Yukun (Beijing) Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PerfusionGo Plus?
The FDA product code for PerfusionGo Plus is LLZ.
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列明Yukun (Beijing) Technology Co., Ltd.为申报人的其他记录
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相关器械（代码：LLZ）
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官方来源
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