COMBOLASER MODEL 5050— 510(k) K893529

Substantially Equivalent

Lasermatic, Inc.

FDA 510(k) clearance K893529 for COMBOLASER MODEL 5050, Substantially Equivalent on 1989-06-08. Applicant: Lasermatic, Inc..

Clearance details

Applicant: Lasermatic, Inc.
Product code: Code GEX
Advisory panel: General, Plastic Surgery
Date received: 1989-05-08
Decision date: 1989-06-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Attleboro, MA, 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.