CILCO ANTERIOR CHAMBER LENS— 510(k) K771933

Substantially Equivalent

California Intraocular Lens

FDA 510(k) clearance K771933 for CILCO ANTERIOR CHAMBER LENS, Substantially Equivalent on 1978-01-26. Applicant: California Intraocular Lens.

Clearance details

Applicant: California Intraocular Lens
Product code: Code HQL
Advisory panel: Ophthalmic
Date received: 1977-10-14
Decision date: 1978-01-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code HQL

product code HQL

Injury: 7,145
Malfunction: 15,684
Other: 5
Total: 22,834

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.