BETASTAR 1131.02 MOBILE OPERATING TABLE— 510(k) K926525

Name: FDA 510(k) clearance K926525
Creator: U.S. Food and Drug Administration
Published: 1993-10-12

Substantially Equivalent

Stierlen-Maquet AG

FDA 510(k) clearance K926525 for BETASTAR 1131.02 MOBILE OPERATING TABLE, Substantially Equivalent on 1993-10-12. Applicant: Stierlen-Maquet AG. Device class: 1.

Clearance details

Applicant: Stierlen-Maquet AG
Product code: Code FQO
Device class: Class 1
Regulation: 21 CFR 878.4960
Advisory panel: General, Plastic Surgery
Date received: 1992-12-30
Decision date: 1993-10-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West-Germany, DE

Download summary PDF View on FDA.gov ↗

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Adverse events under product code FQO

product code FQO

Death: 6
Injury: 145
Malfunction: 685
Total: 836

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.