REPOSABLE INSTRUMENT SYSTEM, MODELS MF001-MF083— 510(k) K014207

Substantially Equivalent

Aesculap, Inc.

FDA 510(k) clearance K014207 for REPOSABLE INSTRUMENT SYSTEM, MODELS MF001-MF083, Substantially Equivalent on 2002-03-21. Applicant: Aesculap, Inc..

Clearance details

Applicant: Aesculap, Inc.
Product code: Code GEI
Advisory panel: General, Plastic Surgery
Date received: 2001-12-21
Decision date: 2002-03-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Center Valley, PA, US

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Adverse events under product code GEI

product code GEI

Death: 133
Injury: 7,585
Malfunction: 35,808
Other: 44
Total: 43,570

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.