NIDEK MODEL VT-4000, MODIFICATION— 510(k) K936302

Name: FDA 510(k) clearance K936302
Creator: U.S. Food and Drug Administration
Published: 1994-07-15

Substantially Equivalent

Nidek, Inc.

FDA 510(k) clearance K936302 for NIDEK MODEL VT-4000, MODIFICATION, Substantially Equivalent on 1994-07-15. Applicant: Nidek, Inc.. Device class: 2.

Clearance details

Applicant: Nidek, Inc.
Product code: Code HQE
Device class: Class 2
Regulation: 21 CFR 886.4150
Advisory panel: Ophthalmic
Date received: 1993-12-29
Decision date: 1994-07-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fremont, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code HQE

product code HQE

Injury: 156
Malfunction: 565
Total: 721

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.