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FDA 510(k)

17HK700G-W

K-Number: K180332 · 2018-06-08

ApplicantLg Electronics
Decision Date2018-06-08
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

17HK700G-W is a medical device manufactured by Lg Electronics. It received FDA 510(k) clearance on 2018-06-08 under approval number K180332. 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 17HK700G-W?

17HK700G-W is a medical device that received FDA 510(k) clearance on 2018-06-08. It is manufactured by Lg Electronics. The 510(k) number is K180332.

When was 17HK700G-W approved by the FDA?

17HK700G-W received FDA 510(k) clearance on 2018-06-08, under approval number K180332.

What company makes 17HK700G-W?

17HK700G-W is manufactured by Lg Electronics.

What is the FDA product code for 17HK700G-W?

The FDA product code for 17HK700G-W is MQB.

Other Devices by Lg Electronics

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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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