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FDA 510(k)

PerfusionGo Plus

K-Number: K221627 · 2023-01-19

ApplicantYukun (Beijing) Technology Co., Ltd.
Decision Date2023-01-19
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PerfusionGo Plus is a medical device manufactured by Yukun (Beijing) Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-01-19 under approval number K221627. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PerfusionGo Plus?

PerfusionGo Plus is a medical device that received FDA 510(k) clearance on 2023-01-19. It is manufactured by Yukun (Beijing) Technology Co., Ltd.. The 510(k) number is K221627.

When was PerfusionGo Plus approved by the FDA?

PerfusionGo Plus received FDA 510(k) clearance on 2023-01-19, under approval number K221627.

What company makes PerfusionGo Plus?

PerfusionGo Plus is manufactured by Yukun (Beijing) Technology Co., Ltd..

What is the FDA product code for PerfusionGo Plus?

The FDA product code for PerfusionGo Plus is LLZ.

Other Devices by Yukun (Beijing) Technology Co., Ltd.

K213986CerebralGo Plus

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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