MODEL DC-1200 DIODE LASER PHOTOCOAGULATOR— 510(k) K895196

Substantially Equivalent

Nidek, Inc.

FDA 510(k) clearance K895196 for MODEL DC-1200 DIODE LASER PHOTOCOAGULATOR, Substantially Equivalent on 1989-10-16. Applicant: Nidek, Inc..

Clearance details

Applicant: Nidek, Inc.
Product code: Code HQF
Advisory panel: Ophthalmic
Date received: 1989-08-11
Decision date: 1989-10-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: El Toro, 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.