DERMA-LASE RUBY LASER - MODEL DLR-1— 510(k) K913256

Substantially Equivalent

Derma-Lase Co.

FDA 510(k) clearance K913256 for DERMA-LASE RUBY LASER - MODEL DLR-1, Substantially Equivalent on 1992-01-22. Applicant: Derma-Lase Co..

Clearance details

Applicant: Derma-Lase Co.
Product code: Code GEX
Advisory panel: General, Plastic Surgery
Date received: 1991-07-16
Decision date: 1992-01-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chicago, IL, US

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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.