DATEX OHMEDA S/5 WEB VIEWER AND S/5 POCKET VIEWER WITH L-WEB03 SOFTWARE— 510(k) K033078

Name: FDA 510(k) clearance K033078
Creator: U.S. Food and Drug Administration
Published: 2003-10-29

Substantially Equivalent

Datex-Ohmeda

FDA 510(k) clearance K033078 for DATEX OHMEDA S/5 WEB VIEWER AND S/5 POCKET VIEWER WITH L-WEB03 SOFTWARE, Substantially Equivalent on 2003-10-29. Applicant: Datex-Ohmeda. Device class: 2.

Clearance details

Applicant: Datex-Ohmeda
Product code: Code MSX
Device class: Class 2
Regulation: 21 CFR 870.2300
Advisory panel: Cardiovascular
Date received: 2003-09-29
Decision date: 2003-10-29
Decision: Substantially Equivalent
Clearance type: Special
Location: Needham, MA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code MSX

product code MSX

Death: 59
Total: 59

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.