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FDA 510(k)

10HQ701G-B

K-Number: K221461 · 2022-07-22

ApplicantLg Electronics.Inc
Decision Date2022-07-22
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

10HQ701G-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 2022-07-22 under 510(k) number K221461. 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 10HQ701G-B?

10HQ701G-B is a medical device that received FDA 510(k) clearance on 2022-07-22. The listed applicant is Lg Electronics.Inc. The 510(k) number is K221461.

When did 10HQ701G-B receive FDA 510(k) clearance?

10HQ701G-B received FDA 510(k) clearance on 2022-07-22, under 510(k) number K221461.

Who is the listed applicant for 10HQ701G-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 10HQ701G-B?

The FDA product code for 10HQ701G-B is MQB.

Other records listing Lg Electronics.Inc as applicant

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Related Devices (Code: MQB)

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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