ASTOFLO PLUS— 510(k) K082765

Name: FDA 510(k) clearance K082765
Creator: U.S. Food and Drug Administration
Published: 2008-12-18

Substantially Equivalent

Stihler Electronic GmbH

FDA 510(k) clearance K082765 for ASTOFLO PLUS, Substantially Equivalent on 2008-12-18. Applicant: Stihler Electronic GmbH. Device class: 2.

Clearance details

Applicant: Stihler Electronic GmbH
Product code: Code LGZ
Device class: Class 2
Regulation: 21 CFR 880.5725
Advisory panel: General Hospital
Date received: 2008-09-22
Decision date: 2008-12-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sound Beach, NY, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code LGZ

product code LGZ

Death: 16
Malfunction: 5,916
Other: 1
Total: 5,933

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.