INTELIPORT OCCLUDING DEVICE— 510(k) K040231

Name: FDA 510(k) clearance K040231
Creator: U.S. Food and Drug Administration
Published: 2004-07-13

Substantially Equivalent

Alcon, Inc.

FDA 510(k) clearance K040231 for INTELIPORT OCCLUDING DEVICE, Substantially Equivalent on 2004-07-13. Applicant: Alcon, Inc.. Device class: Unclassified.

Clearance details

Applicant: Alcon, Inc.
Product code: Code LZU
Device class: Unclassified
Advisory panel: Unknown
Date received: 2004-02-02
Decision date: 2004-07-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Worth, TX, US

Download summary PDF View on FDA.gov ↗

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More clearances from Alcon, Inc.

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Adverse events under product code LZU

product code LZU

Other: 2
Total: 2

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.