DURACLEAN DAILY CLEANER— 510(k) K881987

Name: FDA 510(k) clearance K881987
Creator: U.S. Food and Drug Administration
Published: 1988-06-09

Substantially Equivalent

Allergan Optical

FDA 510(k) clearance K881987 for DURACLEAN DAILY CLEANER, Substantially Equivalent on 1988-06-09. Applicant: Allergan Optical. Device class: 2.

Clearance details

Applicant: Allergan Optical
Product code: Code LPN
Device class: Class 2
Regulation: 21 CFR 886.5928
Advisory panel: Ophthalmic
Date received: 1988-05-11
Decision date: 1988-06-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code LPN

product code LPN

Injury: 333
Other: 8
Total: 341

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.