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FDA 510(k)

AVIEW

K-Number: K171199 · 2018-10-31

ApplicantCoreline Soft Co., Ltd.
Decision Date2018-10-31
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AVIEW is a medical device manufactured by Coreline Soft Co., Ltd.. It received FDA 510(k) clearance on 2018-10-31 under approval number K171199. 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 AVIEW?

AVIEW is a medical device that received FDA 510(k) clearance on 2018-10-31. It is manufactured by Coreline Soft Co., Ltd.. The 510(k) number is K171199.

When was AVIEW approved by the FDA?

AVIEW received FDA 510(k) clearance on 2018-10-31, under approval number K171199.

What company makes AVIEW?

AVIEW is manufactured by Coreline Soft Co., Ltd..

What is the FDA product code for AVIEW?

The FDA product code for AVIEW is LLZ.

Other Devices by Coreline Soft Co., Ltd.

K192040AVIEW Modeler K201710A View LCS K200714AVIEW K193220AVIEW LCS K214036AVIEW K220408AVIEW RT ACS

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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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