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FDA 510(k)

X-Clever (ASHK100G)

K-Number: K233599 · 2024-03-18

ApplicantLg Electronics.Inc
Decision Date2024-03-18
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

X-Clever (ASHK100G) is a medical device manufactured by Lg Electronics.Inc. It received FDA 510(k) clearance on 2024-03-18 under approval number K233599. 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 (ASHK100G)?

X-Clever (ASHK100G) is a medical device that received FDA 510(k) clearance on 2024-03-18. It is manufactured by Lg Electronics.Inc. The 510(k) number is K233599.

When was X-Clever (ASHK100G) approved by the FDA?

X-Clever (ASHK100G) received FDA 510(k) clearance on 2024-03-18, under approval number K233599.

What company makes X-Clever (ASHK100G)?

X-Clever (ASHK100G) is manufactured by Lg Electronics.Inc.

What is the FDA product code for X-Clever (ASHK100G)?

The FDA product code for X-Clever (ASHK100G) 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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