DIODE MEDICAL LASER FAMILY, MODELS 4, 6, 30— 510(k) K072034

Name: FDA 510(k) clearance K072034
Creator: U.S. Food and Drug Administration
Published: 2007-09-20

Substantially Equivalent

Quanta System Spa

FDA 510(k) clearance K072034 for DIODE MEDICAL LASER FAMILY, MODELS 4, 6, 30, Substantially Equivalent on 2007-09-20. Applicant: Quanta System Spa. Device class: 2.

Clearance details

Applicant: Quanta System Spa
Product code: Code GEX
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 2007-07-25
Decision date: 2007-09-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Solbiate Olona (Va), IT

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.