MOBILE OPERATING TABLE 1132.01— 510(k) K970807

Substantially Equivalent

Stierlen-Maquet AG

FDA 510(k) clearance K970807 for MOBILE OPERATING TABLE 1132.01, Substantially Equivalent on 1997-03-14. Applicant: Stierlen-Maquet AG.

Clearance details

Applicant: Stierlen-Maquet AG
Product code: Code GDC
Advisory panel: General, Plastic Surgery
Date received: 1997-03-05
Decision date: 1997-03-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rastatt, DE

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Adverse events under product code GDC

product code GDC

Malfunction: 791
Total: 791

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.