ACKERMANN EUROPCLIP— 510(k) K111930

Name: FDA 510(k) clearance K111930
Creator: U.S. Food and Drug Administration
Published: 2011-11-08

Substantially Equivalent

Ackermann Instrumente GmbH

FDA 510(k) clearance K111930 for ACKERMANN EUROPCLIP, Substantially Equivalent on 2011-11-08. Applicant: Ackermann Instrumente GmbH. Device class: 2.

Clearance details

Applicant: Ackermann Instrumente GmbH
Product code: Code FZP
Device class: Class 2
Regulation: 21 CFR 878.4300
Advisory panel: General, Plastic Surgery
Date received: 2011-07-07
Decision date: 2011-11-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chesterland, OH, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code FZP

product code FZP

Death: 11
Injury: 726
Malfunction: 10,830
Other: 1
Total: 11,568

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.