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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 the device name listed in this FDA 510(k) record. The listed applicant is Lg Electronics.Inc. It received FDA 510(k) clearance on 2018-12-07 under 510(k) 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. The listed applicant is Lg Electronics.Inc. The 510(k) number is K183286.

When did 17HK701G-W receive FDA 510(k) clearance?

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

Who is the listed applicant for 17HK701G-W?

The FDA 510(k) record lists Lg Electronics.Inc as the applicant. This does not by itself establish the device manufacturer.

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

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

Other records listing Lg Electronics.Inc 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.

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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.

K2538000909FCE, 0909FCE-HSRayence Co., Ltd.K260820VIVIX-S 4386W (FXRD-4386WA)Vieworks Co., Ltd.K252996Universal 1417PIKonica Minolta Healthcare Americas, Inc.K252911Lux HD 2530 detector (Lux HD 2530)Iray Imaging Technology (Haining) LimitedK250211Yushan X-Ray Flat Panel DetectorInnocare Optoelectronics Corp.K250665SKR 3000Konica Minolta, 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.

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