DC-3300 LASER DIODE PHOTOCOAGULATOR— 510(k) K013760

Name: FDA 510(k) clearance K013760
Creator: U.S. Food and Drug Administration
Published: 2002-02-11

Substantially Equivalent

Nidek, Inc.

FDA 510(k) clearance K013760 for DC-3300 LASER DIODE PHOTOCOAGULATOR, Substantially Equivalent on 2002-02-11. Applicant: Nidek, Inc.. Device class: 2.

Clearance details

Applicant: Nidek, Inc.
Product code: Code HQF
Device class: Class 2
Regulation: 21 CFR 886.4390
Advisory panel: Ophthalmic
Date received: 2001-11-13
Decision date: 2002-02-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Forest, CA, US

Download summary PDF View on FDA.gov ↗

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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.