LCD Monitors C310S, G310S, C316S, G316S, C616W
K-Number: K240310 · 2024-03-29
Device Summary
Frequently Asked Questions
What is the LCD Monitors C310S, G310S, C316S, G316S, C616W?
LCD Monitors C310S, G310S, C316S, G316S, C616W is a medical device that received FDA 510(k) clearance on 2024-03-29. The listed applicant is Shenzhen Beacon Display Technology Co., Ltd.. The 510(k) number is K240310.
When did LCD Monitors C310S, G310S, C316S, G316S, C616W receive FDA 510(k) clearance?
LCD Monitors C310S, G310S, C316S, G316S, C616W received FDA 510(k) clearance on 2024-03-29, under 510(k) number K240310.
Who is the listed applicant for LCD Monitors C310S, G310S, C316S, G316S, C616W?
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 LCD Monitors C310S, G310S, C316S, G316S, C616W?
The FDA product code for LCD Monitors C310S, G310S, C316S, G316S, C616W 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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.