LENZ CLENZER— 510(k) K881739

Name: FDA 510(k) clearance K881739
Creator: U.S. Food and Drug Administration
Published: 1988-10-07

Substantially Equivalent

Lens Care, Inc.

FDA 510(k) clearance K881739 for LENZ CLENZER, Substantially Equivalent on 1988-10-07. Applicant: Lens Care, Inc.. Device class: 2.

Clearance details

Applicant: Lens Care, Inc.
Product code: Code LYL
Device class: Class 2
Regulation: 21 CFR 886.5928
Advisory panel: Ophthalmic
Date received: 1988-04-25
Decision date: 1988-10-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ft. Lauderdale, FL, US

Download summary PDF View on FDA.gov ↗

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K210300 — VueSonic One Contact Lens Cleaning System, VueSonic Advance 2 Contact Lens Cleaning System2021-04-01
K083757 — BPZ02 MULTIPURPOSE SOLUTION2009-11-18
K021699 — AUTOLENS CLEANING AND DISINFECTING UNIT2002-12-16
K022687 — AOSEPT CLEAR CARE CLEANING AND DISINFECTING SOLUTION2002-11-19

Adverse events under product code LYL

product code LYL

Other: 1
Total: 1

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.