Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

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 a medical device manufactured by Lg Electronics.Inc. It received FDA 510(k) clearance on 2023-01-27 under approval 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. It is manufactured by Lg Electronics.Inc. The 510(k) number is K223546.

When was 14HQ721G-B approved by the FDA?

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

What company makes 14HQ721G-B?

14HQ721G-B is manufactured by Lg Electronics.Inc.

What is the FDA product code for 14HQ721G-B?

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

Other Devices by Lg Electronics.Inc

K18328617HK701G-W K18234814HK701G-W K19186421HK512D K183671LG PRA.L DERMA LED MASK K20177731HN713D K200464LG Pra. L Derma LD Scalp Care

View all 26 devices →

Related Devices (Code: MQB)

K162555EVS 4343, EVS 4343GDRTECH Corporation K162344INNOLUX RICInnolux Corporation K161730Wireless Digital Flat Panel DetectorIray Technology (Shanghai) , Ltd. K162552EVS 3643, EVS 3643GDRTECH Corporation K163019CareView 750Cw/750C X-ray Flat Panel DetectorsCareray Digital Medical System Co., Ltd. K160143ClearVision ExamVue Flat Panel DetectorJpi Healthcare, Inc.

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.

↑