ILUMA VISION MODEL VERSION 2.2— 510(k) K094064

Name: FDA 510(k) clearance K094064
Creator: U.S. Food and Drug Administration
Published: 2010-04-30

Substantially Equivalent

3M Imtec

FDA 510(k) clearance K094064 for ILUMA VISION MODEL VERSION 2.2, Substantially Equivalent on 2010-04-30. Applicant: 3M Imtec. Device class: 2.

Clearance details

Applicant: 3M Imtec
Product code: Code LLZ
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 2009-12-31
Decision date: 2010-04-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, US

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Recent devices under product code LLZ

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Adverse events under product code LLZ

product code LLZ

Death: 13
Total: 13

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.