MD211G3 21.3 DIAGNOSTIC IMAGING LCD MONITOR— 510(k) K122843

Substantially Equivalent

Prodigy Technology Consultant Co., Ltd.

FDA 510(k) clearance K122843 for MD211G3 21.3 DIAGNOSTIC IMAGING LCD MONITOR, Substantially Equivalent on 2012-10-05. Applicant: Prodigy Technology Consultant Co., Ltd..

Clearance details

Applicant: Prodigy Technology Consultant Co., Ltd.
Product code: Code LLZ
Advisory panel: Radiology
Date received: 2012-09-17
Decision date: 2012-10-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taipei, TW

Download summary PDF View on FDA.gov ↗

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.