ATMOS S041 WOUND— 510(k) K090130

Name: FDA 510(k) clearance K090130
Creator: U.S. Food and Drug Administration
Published: 2009-04-02

Substantially Equivalent

Atmos, Inc.

FDA 510(k) clearance K090130 for ATMOS S041 WOUND, Substantially Equivalent on 2009-04-02. Applicant: Atmos, Inc.. Device class: 2.

Clearance details

Applicant: Atmos, Inc.
Product code: Code OMP
Device class: Class 2
Regulation: 21 CFR 878.4780
Advisory panel: General, Plastic Surgery
Date received: 2009-01-21
Decision date: 2009-04-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Denton, TX, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code OMP

product code OMP

Death: 31
Injury: 1,707
Malfunction: 4,047
Other: 1
Total: 5,786

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.