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FDA 510(k)

14HQ721G-B

K-Number: K223546 · 2023-01-27

ApplicantLg Electronics.Inc
Decision Date2023-01-27
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

14HQ721G-B 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 2023-01-27 under 510(k) number K223546. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 14HQ721G-B?

14HQ721G-B is a medical device that received FDA 510(k) clearance on 2023-01-27. The listed applicant is Lg Electronics.Inc. The 510(k) number is K223546.

When did 14HQ721G-B receive FDA 510(k) clearance?

14HQ721G-B received FDA 510(k) clearance on 2023-01-27, under 510(k) number K223546.

Who is the listed applicant for 14HQ721G-B?

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 14HQ721G-B?

The FDA product code for 14HQ721G-B is MQB.

Other records listing Lg Electronics.Inc as applicant

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Related Devices (Code: MQB)

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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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