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FDA 510(k)

14HK701G-W

K-Number: K182348 · 2018-10-18

ApplicantLg Electronics.Inc
Decision Date2018-10-18
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

14HK701G-W is a medical device manufactured by Lg Electronics.Inc. It received FDA 510(k) clearance on 2018-10-18 under approval number K182348. 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 14HK701G-W?

14HK701G-W is a medical device that received FDA 510(k) clearance on 2018-10-18. It is manufactured by Lg Electronics.Inc. The 510(k) number is K182348.

When was 14HK701G-W approved by the FDA?

14HK701G-W received FDA 510(k) clearance on 2018-10-18, under approval number K182348.

What company makes 14HK701G-W?

14HK701G-W is manufactured by Lg Electronics.Inc.

What is the FDA product code for 14HK701G-W?

The FDA product code for 14HK701G-W is MQB.

Other Devices by Lg Electronics.Inc

K18328617HK701G-W K19186421HK512D K183671LG PRA.L DERMA LED MASK K20177731HN713D K200464LG Pra. L Derma LD Scalp Care K19292532HL512D

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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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