NEXT GENERATION LASER— 510(k) K062624

Substantially Equivalent

Alcon Laboratories

FDA 510(k) clearance K062624 for NEXT GENERATION LASER, Substantially Equivalent on 2007-11-05. Applicant: Alcon Laboratories.

Clearance details

Applicant: Alcon Laboratories
Product code: Code HQF
Advisory panel: Ophthalmic
Date received: 2006-09-05
Decision date: 2007-11-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Worth, TX, US

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Adverse events under product code HQF

product code HQF

Injury: 166
Other: 1
Total: 167

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.