17HK700G-W
K-Number: K180332 · 2018-06-08
Device Summary
Frequently Asked Questions
What is the 17HK700G-W?
17HK700G-W is a medical device that received FDA 510(k) clearance on 2018-06-08. The listed applicant is Lg Electronics. The 510(k) number is K180332.
When did 17HK700G-W receive FDA 510(k) clearance?
17HK700G-W received FDA 510(k) clearance on 2018-06-08, under 510(k) number K180332.
Who is the listed applicant for 17HK700G-W?
The FDA 510(k) record lists Lg Electronics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 17HK700G-W?
The FDA product code for 17HK700G-W is MQB.
Other records listing Lg Electronics as applicant
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.
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.
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.