MODEL 8000 ND:YAG LASER SYS TREATMENT OF BENIGN LE— 510(k) K844668

Substantially Equivalent

Cooper Lasersonics, Inc.

FDA 510(k) clearance K844668 for MODEL 8000 ND:YAG LASER SYS TREATMENT OF BENIGN LE, Substantially Equivalent on 1985-01-03. Applicant: Cooper Lasersonics, Inc..

Clearance details

Applicant: Cooper Lasersonics, Inc.
Product code: Code HQF
Advisory panel: Ophthalmic
Date received: 1984-11-30
Decision date: 1985-01-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Clara, CA, 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.