BELIMED STEAM STERILIZER MODEL TOP 5000 SERIES 24— 510(k) K072087

Name: FDA 510(k) clearance K072087
Creator: U.S. Food and Drug Administration
Published: 2007-10-05

Substantially Equivalent

Belimed Sauter AG

FDA 510(k) clearance K072087 for BELIMED STEAM STERILIZER MODEL TOP 5000 SERIES 24, Substantially Equivalent on 2007-10-05. Applicant: Belimed Sauter AG. Device class: 2.

Clearance details

Applicant: Belimed Sauter AG
Product code: Code FLE
Device class: Class 2
Regulation: 21 CFR 880.6880
Advisory panel: General Hospital
Date received: 2007-07-30
Decision date: 2007-10-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sulgen (Tg), CH

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.