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FDA 510(k)

A View LCS

K-Number: K201710 · 2020-10-16

ApplicantCoreline Soft Co., Ltd.
Decision Date2020-10-16
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

A View LCS is a medical device manufactured by Coreline Soft Co., Ltd.. It received FDA 510(k) clearance on 2020-10-16 under approval number K201710. 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 A View LCS?

A View LCS is a medical device that received FDA 510(k) clearance on 2020-10-16. It is manufactured by Coreline Soft Co., Ltd.. The 510(k) number is K201710.

When was A View LCS approved by the FDA?

A View LCS received FDA 510(k) clearance on 2020-10-16, under approval number K201710.

What company makes A View LCS?

A View LCS is manufactured by Coreline Soft Co., Ltd..

What is the FDA product code for A View LCS?

The FDA product code for A View LCS is LLZ.

Other Devices by Coreline Soft Co., Ltd.

K171199AVIEW K192040AVIEW Modeler 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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