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FDA 510(k)

X-Clever

K-Number: K212137 · 2021-12-10

ApplicantLg Electronics.Inc
Decision Date2021-12-10
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

X-Clever is a medical device manufactured by Lg Electronics.Inc. It received FDA 510(k) clearance on 2021-12-10 under approval number K212137. 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 X-Clever?

X-Clever is a medical device that received FDA 510(k) clearance on 2021-12-10. It is manufactured by Lg Electronics.Inc. The 510(k) number is K212137.

When was X-Clever approved by the FDA?

X-Clever received FDA 510(k) clearance on 2021-12-10, under approval number K212137.

What company makes X-Clever?

X-Clever is manufactured by Lg Electronics.Inc.

What is the FDA product code for X-Clever?

The FDA product code for X-Clever is LLZ.

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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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