ALCON MULTI-PURPOSE SOLUTION— 510(k) K071236

Name: FDA 510(k) clearance K071236
Creator: U.S. Food and Drug Administration
Published: 2007-12-12

Substantially Equivalent

Alcon, Inc.

FDA 510(k) clearance K071236 for ALCON MULTI-PURPOSE SOLUTION, Substantially Equivalent on 2007-12-12. Applicant: Alcon, Inc.. Device class: 2.

Clearance details

Applicant: Alcon, Inc.
Product code: Code LPN
Device class: Class 2
Regulation: 21 CFR 886.5928
Advisory panel: Ophthalmic
Date received: 2007-05-03
Decision date: 2007-12-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Worth, TX, 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.