TECNO-GAZ ANDROMEDA VACUUM CS AUTOCLAVE— 510(k) K063681

Name: FDA 510(k) clearance K063681
Creator: U.S. Food and Drug Administration
Published: 2007-06-29

Substantially Equivalent

Mediline Italia S.R.L.

FDA 510(k) clearance K063681 for TECNO-GAZ ANDROMEDA VACUUM CS AUTOCLAVE, Substantially Equivalent on 2007-06-29. Applicant: Mediline Italia S.R.L.. Device class: 2.

Clearance details

Applicant: Mediline Italia S.R.L.
Product code: Code FLE
Device class: Class 2
Regulation: 21 CFR 880.6880
Advisory panel: General Hospital
Date received: 2006-12-11
Decision date: 2007-06-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bethesda, MD, 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.