OXLIFE FREEDOM FIVE OXYGEN CONCENTRATORS, MODEL KXF5— 510(k) K060922

Name: FDA 510(k) clearance K060922
Creator: U.S. Food and Drug Administration
Published: 2006-05-30

Substantially Equivalent

Oxlife, LLC

FDA 510(k) clearance K060922 for OXLIFE FREEDOM FIVE OXYGEN CONCENTRATORS, MODEL KXF5, Substantially Equivalent on 2006-05-30. Applicant: Oxlife, LLC. Device class: 2.

Clearance details

Applicant: Oxlife, LLC
Product code: Code CAW
Device class: Class 2
Regulation: 21 CFR 868.5440
Advisory panel: Anesthesiology
Date received: 2006-04-04
Decision date: 2006-05-30
Decision: Substantially Equivalent
Clearance type: Special
Location: Hendersonville, NC, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code CAW

product code CAW

Death: 204
Injury: 573
Malfunction: 1,400
Other: 6
Total: 2,183

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.