GETINGE 700HC-E SERIES STEAM STERILIZER— 510(k) K120441

Name: FDA 510(k) clearance K120441
Creator: U.S. Food and Drug Administration
Published: 2012-05-31

Substantially Equivalent

Getinge Sourcing, LLC

FDA 510(k) clearance K120441 for GETINGE 700HC-E SERIES STEAM STERILIZER, Substantially Equivalent on 2012-05-31. Applicant: Getinge Sourcing, LLC. Device class: 2.

Clearance details

Applicant: Getinge Sourcing, LLC
Product code: Code FLE
Device class: Class 2
Regulation: 21 CFR 880.6880
Advisory panel: General Hospital
Date received: 2012-02-13
Decision date: 2012-05-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rochester, NY, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code FLE

product code FLE

Malfunction: 444
Total: 444

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.