NIDEK/PHACO EMULSIFICATION SYSTEM MODEL CV-8000— 510(k) K901686

Substantially Equivalent

Nidek, Inc.

FDA 510(k) clearance K901686 for NIDEK/PHACO EMULSIFICATION SYSTEM MODEL CV-8000, Substantially Equivalent on 1990-06-08. Applicant: Nidek, Inc..

Clearance details

Applicant: Nidek, Inc.
Product code: Code HQC
Advisory panel: Ophthalmic
Date received: 1990-04-12
Decision date: 1990-06-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Palo Alto, CA, US

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Adverse events under product code HQC

product code HQC

Injury: 2,378
Malfunction: 8,768
Total: 11,146

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.