PLASMAJET SYSTEM— 510(k) K030819

Name: FDA 510(k) clearance K030819
Creator: U.S. Food and Drug Administration
Published: 2004-08-05

Substantially Equivalent

Plasma Surgical, Ltd.

FDA 510(k) clearance K030819 for PLASMAJET SYSTEM, Substantially Equivalent on 2004-08-05. Applicant: Plasma Surgical, Ltd.. Device class: 2.

Clearance details

Applicant: Plasma Surgical, Ltd.
Product code: Code GEI
Device class: Class 2
Regulation: 21 CFR 878.4400
Advisory panel: General, Plastic Surgery
Date received: 2003-03-14
Decision date: 2004-08-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: London, GB

Download summary PDF View on FDA.gov ↗

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Adverse events under product code GEI

product code GEI

Death: 133
Injury: 7,585
Malfunction: 35,808
Other: 44
Total: 43,570

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.