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FDA 510(k)

2MP Color/Monochrome LCD Monitors C22S+, C22SP+/G22S+, G22SP+, G23S+, G23SP+

K-Number: K201599 · 2020-07-02

Decision Date2020-07-02
Product CodePGY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

2MP Color/Monochrome LCD Monitors C22S+, C22SP+/G22S+, G22SP+, G23S+, G23SP+ is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Beacon Display Technology Co., Ltd.. It received FDA 510(k) clearance on 2020-07-02 under 510(k) number K201599. 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 2MP Color/Monochrome LCD Monitors C22S+, C22SP+/G22S+, G22SP+, G23S+, G23SP+?

2MP Color/Monochrome LCD Monitors C22S+, C22SP+/G22S+, G22SP+, G23S+, G23SP+ is a medical device that received FDA 510(k) clearance on 2020-07-02. The listed applicant is Shenzhen Beacon Display Technology Co., Ltd.. The 510(k) number is K201599.

When did 2MP Color/Monochrome LCD Monitors C22S+, C22SP+/G22S+, G22SP+, G23S+, G23SP+ receive FDA 510(k) clearance?

2MP Color/Monochrome LCD Monitors C22S+, C22SP+/G22S+, G22SP+, G23S+, G23SP+ received FDA 510(k) clearance on 2020-07-02, under 510(k) number K201599.

Who is the listed applicant for 2MP Color/Monochrome LCD Monitors C22S+, C22SP+/G22S+, G22SP+, G23S+, G23SP+?

The FDA 510(k) record lists Shenzhen Beacon Display Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 2MP Color/Monochrome LCD Monitors C22S+, C22SP+/G22S+, G22SP+, G23S+, G23SP+?

The FDA product code for 2MP Color/Monochrome LCD Monitors C22S+, C22SP+/G22S+, G22SP+, G23S+, G23SP+ is PGY.

Other records listing Shenzhen Beacon Display Technology Co., Ltd. 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.

View all 14 devices →

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.