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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 the device name listed in this FDA 510(k) record. The listed applicant is Lg Electronics.Inc. It received FDA 510(k) clearance on 2024-03-18 under 510(k) 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. The listed applicant is Lg Electronics.Inc. The 510(k) number is K233599.

When did X-Clever (ASHK100G) receive FDA 510(k) clearance?

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

Who is the listed applicant for X-Clever (ASHK100G)?

The FDA 510(k) record lists Lg Electronics.Inc as the applicant. This does not by itself establish the device manufacturer.

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

The FDA product code for X-Clever (ASHK100G) is LLZ.

Other records listing Lg Electronics.Inc as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: LLZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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