SUNSOFT (METHAFILCON A) SOFT (HYDROPHILIC) DAILY WEAR CONTACT LENS— 510(k) K964696

Substantially Equivalent

Sunsoft Corp.

FDA 510(k) clearance K964696 for SUNSOFT (METHAFILCON A) SOFT (HYDROPHILIC) DAILY WEAR CONTACT LENS, Substantially Equivalent on 1997-02-20. Applicant: Sunsoft Corp..

Clearance details

Applicant: Sunsoft Corp.
Product code: Code LPL
Advisory panel: Ophthalmic
Date received: 1996-11-22
Decision date: 1997-02-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Albuquerque, NM, 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.