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FDA 510(k)

AccuCTP

K-Number: K220663 · 2022-11-22

ApplicantArteryFlow Technology Co., Ltd.
Decision Date2022-11-22
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AccuCTP is a medical device manufactured by ArteryFlow Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-11-22 under approval number K220663. 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 AccuCTP?

AccuCTP is a medical device that received FDA 510(k) clearance on 2022-11-22. It is manufactured by ArteryFlow Technology Co., Ltd.. The 510(k) number is K220663.

When was AccuCTP approved by the FDA?

AccuCTP received FDA 510(k) clearance on 2022-11-22, under approval number K220663.

What company makes AccuCTP?

AccuCTP is manufactured by ArteryFlow Technology Co., Ltd..

What is the FDA product code for AccuCTP?

The FDA product code for AccuCTP is LLZ.

Other Devices by ArteryFlow Technology Co., Ltd.

K210093AccuFFRangio K213838AneuGuide K231353AccuCTP Pro K230303AccuFFRangio Plus K221711AccuICAS

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Official Source

View on FDA Database →

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

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