3MP (X213C3P0E, X213G3P0E) and 2MP (X213C2P0E, X213G2P0E) LCD Display— 510(k) K151854

Name: FDA 510(k) clearance K151854
Creator: U.S. Food and Drug Administration
Published: 2015-07-28

Substantially Equivalent

D-View Display Technology Co., Ltd.

FDA 510(k) clearance K151854 for 3MP (X213C3P0E, X213G3P0E) and 2MP (X213C2P0E, X213G2P0E) LCD Display, Substantially Equivalent on 2015-07-28. Applicant: D-View Display Technology Co., Ltd.. Device class: 2.

Clearance details

Applicant: D-View Display Technology Co., Ltd.
Product code: Code LLZ
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 2015-07-07
Decision date: 2015-07-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bei Jing, CN

Download summary PDF View on FDA.gov ↗

Recent devices under product code LLZ

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Adverse events under product code LLZ

product code LLZ

Death: 13
Total: 13

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.