DC 7— 510(k) K131839

Name: FDA 510(k) clearance K131839
Creator: U.S. Food and Drug Administration
Published: 2013-11-07

Substantially Equivalent

Dc International, LLC

FDA 510(k) clearance K131839 for DC 7, Substantially Equivalent on 2013-11-07. Applicant: Dc International, LLC. Device class: 2.

Clearance details

Applicant: Dc International, LLC
Product code: Code GEX
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 2013-06-21
Decision date: 2013-11-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wellington, FL, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code GEX

product code GEX

Death: 33
Injury: 3,045
Malfunction: 12,903
Other: 25
Total: 16,006

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.