VISTAKON MULTIFOCAL (ETAFILCON A) CONTACT LENS— 510(k) K953804

Substantially Equivalent

Vistakon, Johnson & Johnson Vision Products, Inc.

FDA 510(k) clearance K953804 for VISTAKON MULTIFOCAL (ETAFILCON A) CONTACT LENS, Substantially Equivalent on 1995-09-26. Applicant: Vistakon, Johnson & Johnson Vision Products, Inc..

Clearance details

Applicant: Vistakon, Johnson & Johnson Vision Products, Inc.
Product code: Code LPL
Advisory panel: Ophthalmic
Date received: 1995-08-08
Decision date: 1995-09-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jacksonville, FL, US

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Adverse events under product code LPL

product code LPL

Injury: 988
Other: 4
Total: 992

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.