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FDA 510(k)

LCD Monitor (MD310C, MD310G, MD210G)

K-Number: K170944 · 2017-05-25

ApplicantBenq Corporation
Decision Date2017-05-25
Product CodePGY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LCD Monitor (MD310C, MD310G, MD210G) is the device name listed in this FDA 510(k) record. The listed applicant is Benq Corporation. It received FDA 510(k) clearance on 2017-05-25 under 510(k) number K170944. The device is classified under product code PGY. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LCD Monitor (MD310C, MD310G, MD210G)?

LCD Monitor (MD310C, MD310G, MD210G) is a medical device that received FDA 510(k) clearance on 2017-05-25. The listed applicant is Benq Corporation. The 510(k) number is K170944.

When did LCD Monitor (MD310C, MD310G, MD210G) receive FDA 510(k) clearance?

LCD Monitor (MD310C, MD310G, MD210G) received FDA 510(k) clearance on 2017-05-25, under 510(k) number K170944.

Who is the listed applicant for LCD Monitor (MD310C, MD310G, MD210G)?

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

What is the FDA product code for LCD Monitor (MD310C, MD310G, MD210G)?

The FDA product code for LCD Monitor (MD310C, MD310G, MD210G) is PGY.

Related Devices (Code: PGY)

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.

K261213Medical Monitor (40HT513D)Lg Electronics.IncK252780LCD Monitor (CL1902A, CL2103F)Shenzhen Beacon Display Technology Co., Ltd.K253242LCD Monitor (C1216W, C822W, C821W)Shenzhen Beacon Display Technology Co., Ltd.K252030RadiForce GX570; RadiForce GX570-AREizo CorporationK243221RadiForce RX570; RadiForce RX570-AREizo CorporationK243031LCD Monitors C310S, G310S, C316S, G316S, C616WShenzhen Beacon Display Technology Co., Ltd.

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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