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)

17HK701G-W

K-Number: K183286 · 2018-12-07

ApplicantLg Electronics.Inc
Decision Date2018-12-07
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

17HK701G-W is a medical device manufactured by Lg Electronics.Inc. It received FDA 510(k) clearance on 2018-12-07 under approval number K183286. 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 17HK701G-W?

17HK701G-W is a medical device that received FDA 510(k) clearance on 2018-12-07. It is manufactured by Lg Electronics.Inc. The 510(k) number is K183286.

When was 17HK701G-W approved by the FDA?

17HK701G-W received FDA 510(k) clearance on 2018-12-07, under approval number K183286.

What company makes 17HK701G-W?

17HK701G-W is manufactured by Lg Electronics.Inc.

What is the FDA product code for 17HK701G-W?

The FDA product code for 17HK701G-W is MQB.

Other Devices by Lg Electronics.Inc

K18234814HK701G-W K19186421HK512D K183671LG PRA.L DERMA LED MASK K20177731HN713D K200464LG Pra. L Derma LD Scalp Care K19292532HL512D

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.

↑