21.3 INCH MONOCHROME DIGITAL MAMMOGRAPHY LCD MONITOR MS55I2 (ML21055, MD211G5)— 510(k) K131137

Name: FDA 510(k) clearance K131137
Creator: U.S. Food and Drug Administration
Published: 2013-07-18

Substantially Equivalent

Jvckenwood Corporation

FDA 510(k) clearance K131137 for 21.3 INCH MONOCHROME DIGITAL MAMMOGRAPHY LCD MONITOR MS55I2 (ML21055, MD211G5), Substantially Equivalent on 2013-07-18. Applicant: Jvckenwood Corporation. Device class: 2.

Clearance details

Applicant: Jvckenwood Corporation
Product code: Code LLZ
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 2013-04-23
Decision date: 2013-07-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Nagano-Ken, JP

Download summary PDF View on FDA.gov ↗

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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.