CILCO ANTERIOR CHAMBER LENS— 510(k) K771933

Name: FDA 510(k) clearance K771933
Creator: U.S. Food and Drug Administration
Published: 1978-01-26

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. Device class: 3.

Clearance details

Applicant: California Intraocular Lens
Product code: Code HQL
Device class: Class 3
Regulation: 21 CFR 886.3600
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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Recent devices under product code HQL

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K914311 — CHIROFLEX II LENS MICROSERT(TM)1992-01-27
K913626 — SOFTRANS INJECTOR1991-12-18
K842892 — NIDEK DIGITAL KERATOMETER1984-10-05
K842504 — AMER. MEDICAL OPTICS DIGITAL KERATO-1984-10-01

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.